A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566023



Internal ID16006746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103595309..103731914hg38UCSC Ensembl
Innerchr14:104061646..104198251hg19UCSC Ensembl
Innerchr14:103131399..103268004hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38136606
hg19136606
hg18136606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834399
Samples
Known GenesKLC1, XRCC3, ZFYVE21
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566023
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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