A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052880



Internal ID19142099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68053967..68237516hg38UCSC Ensembl
Innerchr13:68628099..68811648hg19UCSC Ensembl
Innerchr13:67526100..67709649hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38183550
hg19183550
hg18183550
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1702n100
Supporting Variantsnssv3527941
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)nsv1052880
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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