A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv958867



Internal ID16252823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8784337..8812029hg38UCSC Ensembl
Innerchr3:8826023..8853715hg19UCSC Ensembl
Innerchr3:8801023..8828715hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3827693
hg1927693
hg1827693
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589629
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)nssv958867
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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