A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv805973



Internal ID16099929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18594359..18922294hg38UCSC Ensembl
Innerchr13:19168499..19496434hg19UCSC Ensembl
Innerchr13:18066499..18394434hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38327936
hg19327936
hg18327936
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561154
Supporting Variants
Samples
Known GenesANKRD20A9P, LINC00408, LINC00417
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv805973
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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