A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149464



Internal ID15876739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:114171819..114212223hg38UCSC Ensembl
Innerchr13:114937294..114977698hg19UCSC Ensembl
Innerchr13:113955396..113995800hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3840405
hg1940405
hg1840405
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563520
Supporting Variants
SamplesHGDP00886
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149464
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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