A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv971532



Internal ID15918802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:112425179..112552010hg38UCSC Ensembl
Innerchr3:112144026..112270857hg19UCSC Ensembl
Innerchr3:113626716..113753547hg18UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38126832
hg19126832
hg18126832
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591300
Supporting Variants
Samples
Known GenesATG3, BTLA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv971532
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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