A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565884



Internal ID16353293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101700166..101713702hg38UCSC Ensembl
Innerchr14:102166503..102180039hg19UCSC Ensembl
Innerchr14:101236256..101249792hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3813537
hg1913537
hg1813537
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv833729, nssv833728
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565884
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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