A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv878450



Internal ID16172406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14194215..14281865hg38UCSC Ensembl
Innerchr18:14194214..14281864hg19UCSC Ensembl
Innerchr18:14184214..14271864hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3887651
hg1987651
hg1887651
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576532
Supporting Variants
Samples
Known GenesANKRD20A5P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv878450
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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