A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3527559



Internal ID18825840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18821486..18844391hg38UCSC Ensembl
Innerchr13:19395626..19418531hg19UCSC Ensembl
Innerchr13:18293626..18316531hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg3822906
hg1922906
hg1822906
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043732
Supporting Variants
Samples
Known GenesANKRD20A9P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3527559
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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