A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565630



Internal ID16353039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:95282378..95320320hg38UCSC Ensembl
Innerchr14:95748715..95786657hg19UCSC Ensembl
Innerchr14:94818468..94856410hg18UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3837943
hg1937943
hg1837943
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv832705
Samples
Known GenesCLMN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565630
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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