A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698188



Internal ID15088154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41286691..41318043hg38UCSC Ensembl
Innerchr3:41328182..41359534hg19UCSC Ensembl
Innerchr3:41303186..41334538hg18UCSC Ensembl
Innerchr3:41303186..41334538hg17UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3831353
hg1931353
hg1831353
hg1731353
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521572
Supporting Variants
Samples
Known GenesULK4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698188
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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