A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565207



Internal ID16352616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:76552223..76610820hg38UCSC Ensembl
Innerchr14:77018566..77077163hg19UCSC Ensembl
Innerchr14:76088319..76146916hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3858598
hg1958598
hg1858598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv829558
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565207
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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