A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834064



Internal ID16128020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101711842..101735235hg38UCSC Ensembl
Innerchr14:102178179..102201572hg19UCSC Ensembl
Innerchr14:101247932..101271325hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3823394
hg1923394
hg1823394
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565911
Supporting Variants
Samples
Known GenesLINC00239
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv834064
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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