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nsv5475643

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,269

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 124 SVs from 27 studies. See in: genome view    
Submitted genomic135,001,394-135,011,662Question Mark
Overlapping variant regions from other studies: 124 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):134,686,145-134,696,413Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5475643Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7135,001,394135,011,662
nsv5475643RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7134,686,145134,696,413

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17003657duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17003657Submitted genomicNC_000007.14:g.135
001394_135011662du
p
GRCh38 (hg38)NC_000007.14Chr7135,001,394135,011,662
nssv17003657RemappedPerfectNC_000007.13:g.134
686145_134696413du
p
GRCh37.p13First PassNC_000007.13Chr7134,686,145134,696,413

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)
nssv17003657<0.00116404
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