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nsv4212664

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:185

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 27 SVs from 3 studies. See in: genome view    
Remapped(Score: Perfect):75,661,329-75,661,513Question Mark
Overlapping variant regions from other studies: 27 SVs from 3 studies. See in: genome view    
Submitted genomic76,127,672-76,127,856Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4212664RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000014.9Chr1475,661,32975,661,513
nsv4212664Submitted genomicGRCh37.p13Primary AssemblyNC_000014.8Chr1476,127,67276,127,856

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15820446deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15820446RemappedPerfectNC_000014.9:g.7566
1329_75661513del
GRCh38.p12First PassNC_000014.9Chr1475,661,32975,661,513
nssv15820446Submitted genomicNC_000014.8:g.7612
7672_76127856del
GRCh37.p13NC_000014.8Chr1476,127,67276,127,856

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv158204464.6e-005121694
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