A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv958892



Internal ID16252848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8804661..8814440hg38UCSC Ensembl
Innerchr3:8846347..8856126hg19UCSC Ensembl
Innerchr3:8821347..8831126hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg389780
hg199780
hg189780
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589644
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv958892
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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