A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037082



Internal ID18779613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:20932196..21204957hg38UCSC Ensembl
Innerchr13:21506335..21779096hg19UCSC Ensembl
Innerchr13:20404335..20677096hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38272762
hg19272762
hg18272762
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523134
Samples
Known GenesLATS2, LINC00367, MRP63, SAP18, SKA3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037082
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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