A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564637



Internal ID16352046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:43353396..43709851hg38UCSC Ensembl
Innerchr14:43822599..44179054hg19UCSC Ensembl
Innerchr14:42892349..43248804hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38356456
hg19356456
hg18356456
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3681n54
Supporting Variantsnssv827519
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564637
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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