A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565372



Internal ID16352781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:83405209..83503574hg38UCSC Ensembl
Innerchr14:83871553..83969918hg19UCSC Ensembl
Innerchr14:82941306..83039671hg18UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg3898366
hg1998366
hg1898366
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv831389
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565372
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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