A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564653



Internal ID16352062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:43883079..44389384hg38UCSC Ensembl
Innerchr14:44352282..44858587hg19UCSC Ensembl
Innerchr14:43422032..43928337hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38506306
hg19506306
hg18506306
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv827538
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564653
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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