A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565431



Internal ID16352840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:85813876..85855940hg38UCSC Ensembl
Innerchr14:86280220..86322284hg19UCSC Ensembl
Innerchr14:85349973..85392037hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3842065
hg1942065
hg1842065
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3826n54
Supporting Variantsnssv831945
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565431
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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