A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698210



Internal ID15434862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:110413833..110425441hg38UCSC Ensembl
Innerchr9:113176113..113187721hg19UCSC Ensembl
Innerchr9:112215934..112227542hg18UCSC Ensembl
Innerchr9:110255668..110267276hg17UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3811609
hg1911609
hg1811609
hg1711609
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521593
Supporting Variants
Samples
Known GenesSVEP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698210
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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