A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564397



Internal ID16351806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:38066968..38089720hg38UCSC Ensembl
Innerchr14:38536173..38558925hg19UCSC Ensembl
Innerchr14:37605924..37628676hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3822753
hg1922753
hg1822753
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv826005
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564397
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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