A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565876



Internal ID16353285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101457829..101459031hg38UCSC Ensembl
Innerchr14:101924166..101925368hg19UCSC Ensembl
Innerchr14:100993919..100995121hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg381203
hg191203
hg181203
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv833711
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565876
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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