A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1107457



Internal ID15613957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18996430..19031299hg38UCSC Ensembl
Innerchr8:18853940..18888809hg19UCSC Ensembl
Innerchr8:18898220..18933089hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3834870
hg1934870
hg1834870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610743
Supporting Variants
Samples
Known GenesPSD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1107457
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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