A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3527557



Internal ID18825838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18631932..18864679hg38UCSC Ensembl
Innerchr13:19206072..19438819hg19UCSC Ensembl
Innerchr13:18104072..18336819hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38232748
hg19232748
hg18232748
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048594
Supporting Variants
Samples
Known GenesANKRD20A9P, LINC00417
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3527557
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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