A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565376



Internal ID16352785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:84145744..84178478hg38UCSC Ensembl
Innerchr14:84612088..84644822hg19UCSC Ensembl
Innerchr14:83681841..83714575hg18UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg3832735
hg1932735
hg1832735
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv831393
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565376
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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