A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151869



Internal ID15527169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:10464960..10471730hg38UCSC Ensembl
Innerchr3:10506644..10513414hg19UCSC Ensembl
Innerchr3:10481644..10488414hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg386771
hg196771
hg186771
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589653
Supporting Variants
SamplesHGDP00402
Known GenesATP2B2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151869
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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