A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591907



Internal ID16032630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:141876489..141877262hg38UCSC Ensembl
Innerchr3:141595331..141596104hg19UCSC Ensembl
Innerchr3:143078021..143078794hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38774
hg19774
hg18774
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv975200, nssv975199, nssv975202, nssv975201
Samples
Known GenesATP1B3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591907
Frequency
Sample Size17421
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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