A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv973976



Internal ID16267932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:132118446..132146943hg38UCSC Ensembl
Innerchr3:131837290..131865787hg19UCSC Ensembl
Innerchr3:133319980..133348477hg18UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3828498
hg1928498
hg1828498
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591772
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)nssv973976
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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