A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682470



Internal ID15419122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:106656499..106667519hg38UCSC Ensembl
Innerchr6:107104374..107115394hg19UCSC Ensembl
Innerchr6:107211067..107222087hg18UCSC Ensembl
Innerchr6:107211067..107222087hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3811021
hg1911021
hg1811021
hg1711021
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516902
Supporting Variants
Samples
Known GenesQRSL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682470
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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