A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv827659



Internal ID16121615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:44715831..44765525hg38UCSC Ensembl
Innerchr14:45185034..45234728hg19UCSC Ensembl
Innerchr14:44254784..44304478hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3849695
hg1949695
hg1849695
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564717
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv827659
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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