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nsv5509179

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,301,711

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 19588 SVs from 122 studies. See in: genome view    
Submitted genomic106,441,255-114,742,965Question Mark
Overlapping variant regions from other studies: 19594 SVs from 122 studies. See in: genome view    
Remapped(Score: Perfect):106,311,982-114,613,687Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5509179Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11106,441,255114,742,965
nsv5509179RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11106,311,982114,613,687

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17050590deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17050590Submitted genomicNC_000011.10:g.106
441255_114742965de
l
GRCh38 (hg38)NC_000011.10Chr11106,441,255114,742,965
nssv17050590RemappedPerfectNC_000011.9:g.1063
11982_114613687del
GRCh37.p13First PassNC_000011.9Chr11106,311,982114,613,687

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)
nssv17050590<0.00116404
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