A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591902



Internal ID16032625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:141875705..141877262hg38UCSC Ensembl
Innerchr3:141594547..141596104hg19UCSC Ensembl
Innerchr3:143077237..143078794hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381558
hg191558
hg181558
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv975191
Samples
Known GenesATP1B3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591902
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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