A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565763



Internal ID16006486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:99683165..99767016hg38UCSC Ensembl
Innerchr14:100149502..100233353hg19UCSC Ensembl
Innerchr14:99219255..99303106hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3883852
hg1983852
hg1883852
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv833046
Samples
Known GenesCYP46A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565763
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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