A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565862



Internal ID16353271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101184215..101213659hg38UCSC Ensembl
Innerchr14:101650552..101679996hg19UCSC Ensembl
Innerchr14:100720305..100749749hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3829445
hg1929445
hg1829445
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148704
Samples1780862094_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565862
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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