A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv825077



Internal ID16119033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27838876..28188182hg38UCSC Ensembl
Innerchr14:28308082..28657388hg19UCSC Ensembl
Innerchr14:27377922..27727139hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38349307
hg19349307
hg18349218
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564137
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv825077
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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