A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv975192



Internal ID15922462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:141876438..141877068hg38UCSC Ensembl
Innerchr3:141595280..141595910hg19UCSC Ensembl
Innerchr3:143077970..143078600hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38631
hg19631
hg18631
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591903
Supporting Variants
Samples
Known GenesATP1B3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv975192
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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