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nsv6290085

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:25,723

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1240 SVs from 93 studies. See in: genome view    
Remapped(Score: Perfect):195,692,297-195,717,322Question Mark
Overlapping variant regions from other studies: 787 SVs from 67 studies. See in: genome view    
Remapped(Score: Perfect):78,722-103,747Question Mark
Overlapping variant regions from other studies: 768 SVs from 66 studies. See in: genome view    
Remapped(Score: Good):76,873-100,665Question Mark
Overlapping variant regions from other studies: 798 SVs from 68 studies. See in: genome view    
Remapped(Score: Perfect):62,794-87,819Question Mark
Overlapping variant regions from other studies: 774 SVs from 67 studies. See in: genome view    
Remapped(Score: Good):76,871-101,377Question Mark
Overlapping variant regions from other studies: 772 SVs from 67 studies. See in: genome view    
Remapped(Score: Good):77,092-102,814Question Mark
Overlapping variant regions from other studies: 798 SVs from 68 studies. See in: genome view    
Remapped(Score: Perfect):62,794-87,819Question Mark
Overlapping variant regions from other studies: 758 SVs from 66 studies. See in: genome view    
Remapped(Score: Pass):76,875-100,103Question Mark
Overlapping variant regions from other studies: 1244 SVs from 94 studies. See in: genome view    
Submitted genomic195,419,168-195,444,193Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv6290085RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3195,692,297195,717,322
nsv6290085RemappedPerfectGRCh38.p12ALT_REF_LOCI_3Second PassNT_187678.1Chr3|NT_18
7678.1		78,722103,747
nsv6290085RemappedGoodGRCh38.p12ALT_REF_LOCI_4Second PassNT_187688.1Chr3|NT_18
7688.1		76,873100,665
nsv6290085RemappedPerfectGRCh38.p12ALT_REF_LOCI_5Second PassNT_187689.1Chr3|NT_18
7689.1		62,79487,819
nsv6290085RemappedGoodGRCh38.p12ALT_REF_LOCI_6Second PassNT_187690.1Chr3|NT_18
7690.1		76,871101,377
nsv6290085RemappedGoodGRCh38.p12ALT_REF_LOCI_7Second PassNT_187691.1Chr3|NT_18
7691.1		77,092102,814
nsv6290085RemappedPerfectGRCh38.p12ALT_REF_LOCI_1Second PassNT_187532.1Chr3|NT_18
7532.1		62,79487,819
nsv6290085RemappedPassGRCh38.p12ALT_REF_LOCI_2Second PassNT_187649.1Chr3|NT_18
7649.1		76,875100,103
nsv6290085Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3195,419,168195,444,193

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17955711copy number lossOligo aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv17955711RemappedPerfectNT_187689.1:g.(?_6
2794)_(87819_?)del		GRCh38.p12Second PassNT_187689.1Chr3|NT_18
7689.1		62,79487,819
nssv17955711RemappedGoodNT_187690.1:g.(?_7
6871)_(101377_?)de
l		GRCh38.p12Second PassNT_187690.1Chr3|NT_18
7690.1		76,871101,377
nssv17955711RemappedGoodNT_187688.1:g.(?_7
6873)_(100665_?)de
l		GRCh38.p12Second PassNT_187688.1Chr3|NT_18
7688.1		76,873100,665
nssv17955711RemappedGoodNT_187691.1:g.(?_7
7092)_(102814_?)de
l		GRCh38.p12Second PassNT_187691.1Chr3|NT_18
7691.1		77,092102,814
nssv17955711RemappedPerfectNT_187678.1:g.(?_7
8722)_(103747_?)de
l		GRCh38.p12Second PassNT_187678.1Chr3|NT_18
7678.1		78,722103,747
nssv17955711RemappedPerfectNT_187532.1:g.(?_6
2794)_(87819_?)del		GRCh38.p12Second PassNT_187532.1Chr3|NT_18
7532.1		62,79487,819
nssv17955711RemappedPassNT_187649.1:g.(?_7
6875)_(100103_?)de
l		GRCh38.p12Second PassNT_187649.1Chr3|NT_18
7649.1		76,875100,103
nssv17955711RemappedPerfectNC_000003.12:g.(?_
195692297)_(195717
322_?)del		GRCh38.p12First PassNC_000003.12Chr3195,692,297195,717,322
nssv17955711Submitted genomicNC_000003.11:g.(?_
195419168)_(195444
193_?)del		GRCh37 (hg19)NC_000003.11Chr3195,419,168195,444,193

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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