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nsv5479368

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:101

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 117 SVs from 25 studies. See in: genome view    
Submitted genomic123,139,210-123,139,310Question Mark
Overlapping variant regions from other studies: 117 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):122,779,264-122,779,364Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5479368Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7123,139,210123,139,310
nsv5479368RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7122,779,264122,779,364

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17003455deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17003455Submitted genomicNC_000007.14:g.123
139210_123139310de
l
GRCh38 (hg38)NC_000007.14Chr7123,139,210123,139,310
nssv17003455RemappedPerfectNC_000007.13:g.122
779264_122779364de
l
GRCh37.p13First PassNC_000007.13Chr7122,779,264122,779,364

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)
nssv17003455<0.00126404
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