A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561155



Internal ID16348564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18614476..18920846hg38UCSC Ensembl
Innerchr13:19188616..19494986hg19UCSC Ensembl
Innerchr13:18086616..18392986hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38306371
hg19306371
hg18306371
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3061n54
Supporting Variantsnssv805974
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)nsv561155
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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