A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv829096



Internal ID15776366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73001051..73063970hg38UCSC Ensembl
Innerchr14:73467759..73530678hg19UCSC Ensembl
Innerchr14:72537512..72600431hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3862920
hg1962920
hg1862920
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565050
Supporting Variants
Samples
Known GenesRBM25, ZFYVE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv829096
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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