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nsv5507908

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:79

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 128 SVs from 24 studies. See in: genome view    
Submitted genomic37,576,736-37,576,814Question Mark
Overlapping variant regions from other studies: 128 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):38,150,873-38,150,951Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5507908Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1337,576,73637,576,814
nsv5507908RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1338,150,87338,150,951

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17686955deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17686955Submitted genomicNC_000013.11:g.375
76736_37576814del
GRCh38 (hg38)NC_000013.11Chr1337,576,73637,576,814
nssv17686955RemappedPerfectNC_000013.10:g.381
50873_38150951del
GRCh37.p13First PassNC_000013.10Chr1338,150,87338,150,951

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)
nssv17686955<0.00136404
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