A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565375



Internal ID16352784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:83833322..83870600hg38UCSC Ensembl
Innerchr14:84299666..84336944hg19UCSC Ensembl
Innerchr14:83369419..83406697hg18UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg3837279
hg1937279
hg1837279
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv831392
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565375
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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