A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565598



Internal ID16353007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:93988074..93988969hg38UCSC Ensembl
Innerchr14:94454420..94455315hg19UCSC Ensembl
Innerchr14:93524173..93525068hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg38896
hg19896
hg18896
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3854n54
Supporting Variantsnssv832582, nssv832581
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565598
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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