A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148626



Internal ID15876222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:51295971..51328705hg38UCSC Ensembl
Innerchr14:51762689..51795423hg19UCSC Ensembl
Innerchr14:50832439..50865173hg18UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg3832735
hg1932735
hg1832735
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564841
Supporting Variants
SamplesHGDP00805
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148626
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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