A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565627



Internal ID16353036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:94673523..94686776hg38UCSC Ensembl
Innerchr14:95139860..95153113hg19UCSC Ensembl
Innerchr14:94209613..94222866hg18UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3813254
hg1913254
hg1813254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv832704
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565627
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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