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nsv2790584

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,940

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 549 SVs from 66 studies. See in: genome view    
Submitted genomic107,365,916-107,376,855Question Mark
Overlapping variant regions from other studies: 549 SVs from 66 studies. See in: genome view    
Remapped(Score: Perfect):107,236,642-107,247,581Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv2790584Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11107,365,916107,376,855
nsv2790584RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11107,236,642107,247,581

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv13689854deletionSequencingGenotyping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv13689854Submitted genomicNC_000011.10:g.107
365916_107376855de
l10940
GRCh38 (hg38)NC_000011.10Chr11107,365,916107,376,855
nssv13689854RemappedPerfectNC_000011.9:g.1072
36642_107247581del
10940
GRCh37.p13First PassNC_000011.9Chr11107,236,642107,247,581

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)
nssv136898540.3792258
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