A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv805972



Internal ID16099928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18589694..18842946hg38UCSC Ensembl
Innerchr13:19163834..19417086hg19UCSC Ensembl
Innerchr13:18061834..18315086hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38253253
hg19253253
hg18253253
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561153
Supporting Variants
Samples
Known GenesANKRD20A9P, LINC00417
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv805972
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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