A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565502



Internal ID16352911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:87172650..87242640hg38UCSC Ensembl
Innerchr14:87638994..87708984hg19UCSC Ensembl
Innerchr14:86708747..86778737hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3869991
hg1969991
hg1869991
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv832159, nssv832160
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565502
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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