A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051362



Internal ID19140581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:80629953..81982184hg38UCSC Ensembl
Innerchr13:81204088..82556319hg19UCSC Ensembl
Innerchr13:80102089..81454320hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg381352232
hg191352232
hg181352232
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3530529
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051362
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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