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nsv833263

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:210,831

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 492 SVs from 48 studies. See in: genome view    
Remapped(Score: Perfect):65,997,410-66,208,240Question Mark
Overlapping variant regions from other studies: 492 SVs from 48 studies. See in: genome view    
Remapped(Score: Perfect):66,031,313-66,242,143Question Mark
Overlapping variant regions from other studies: 42 SVs from 3 studies. See in: genome view    
Submitted genomic64,588,814-64,799,644Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv833263RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000016.10Chr1665,997,41066,208,240
nsv833263RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1666,031,31366,242,143
nsv833263Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000016.8Chr1664,588,81464,799,644

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1452822copy number lossBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1452822RemappedPerfectNC_000016.10:g.(65
997410_?)_(?_66208
240)del
GRCh38.p12First PassNC_000016.10Chr1665,997,41066,208,240
nssv1452822RemappedPerfectNC_000016.9:g.(660
31313_?)_(?_662421
43)del
GRCh37.p13First PassNC_000016.9Chr1666,031,31366,242,143
nssv1452822Submitted genomicNC_000016.8:g.(645
88814_?)_(?_647996
44)del
NCBI35 (hg17)NC_000016.8Chr1664,588,81464,799,644

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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