A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696935



Internal ID15086901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18996430..19031299hg38UCSC Ensembl
Innerchr8:18853940..18888809hg19UCSC Ensembl
Innerchr8:18898220..18933089hg18UCSC Ensembl
Innerchr8:18898220..18933089hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3834870
hg1934870
hg1834870
hg1734870
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519585
Supporting Variants
Samples
Known GenesPSD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696935
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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