A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654896



Internal ID15391548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:201243708..201245626hg38UCSC Ensembl
Innerchr1:201212836..201214754hg19UCSC Ensembl
Innerchr1:199479459..199481377hg18UCSC Ensembl
Innerchr1:197944493..197946411hg17UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg381919
hg191919
hg181919
hg171919
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515827
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv654896
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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