A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051550



Internal ID19140769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:71906455..71930680hg38UCSC Ensembl
Innerchr13:72480593..72504818hg19UCSC Ensembl
Innerchr13:71378594..71402819hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3824226
hg1924226
hg1824226
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3530499
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)nsv1051550
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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