A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565861



Internal ID16353270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101167739..101187021hg38UCSC Ensembl
Innerchr14:101634076..101653358hg19UCSC Ensembl
Innerchr14:100703829..100723111hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3819283
hg1919283
hg1819283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv833680
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565861
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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