A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565371



Internal ID16352780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:83391178..83427140hg38UCSC Ensembl
Innerchr14:83857522..83893484hg19UCSC Ensembl
Innerchr14:82927275..82963237hg18UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg3835963
hg1935963
hg1835963
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3817n54
Supporting Variantsnssv831387, nssv831388
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565371
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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