A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564736



Internal ID16352145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:46062769..46330787hg38UCSC Ensembl
Innerchr14:46531972..46799990hg19UCSC Ensembl
Innerchr14:45601722..45869740hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38268019
hg19268019
hg18268019
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148605
SamplesHGDP01416
Known GenesLINC00871
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564736
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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