A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148695



Internal ID15876362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:40441476..40460102hg38UCSC Ensembl
Innerchr14:40910680..40929306hg19UCSC Ensembl
Innerchr14:39980430..39999056hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3818627
hg1918627
hg1818627
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564459
Supporting Variants
SamplesHGDP00828
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148695
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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