A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565649



Internal ID16006372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:96377253..96453283hg38UCSC Ensembl
Innerchr14:96843590..96919620hg19UCSC Ensembl
Innerchr14:95913343..95989373hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3876031
hg1976031
hg1876031
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv832729
Samples
Known GenesAK7, GSKIP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565649
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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