A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591906



Internal ID16032629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:141876489..141876995hg38UCSC Ensembl
Innerchr3:141595331..141595837hg19UCSC Ensembl
Innerchr3:143078021..143078527hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38507
hg19507
hg18507
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv975196, nssv975197, nssv975198
Samples
Known GenesATP1B3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591906
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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