A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv973020



Internal ID16266976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:128662243..128694054hg38UCSC Ensembl
Innerchr3:128381086..128412897hg19UCSC Ensembl
Innerchr3:129863776..129895587hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3831812
hg1931812
hg1831812
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591616
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)nssv973020
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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