A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591910



Internal ID16032633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:141876771..141877262hg38UCSC Ensembl
Innerchr3:141595613..141596104hg19UCSC Ensembl
Innerchr3:143078303..143078794hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38492
hg19492
hg18492
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv975205
Samples
Known GenesATP1B3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591910
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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