A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052522



Internal ID19141741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107460700..107474020hg38UCSC Ensembl
Innerchr11:107331426..107344746hg19UCSC Ensembl
Innerchr11:106836636..106849956hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3813321
hg1913321
hg1813321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1273n100
Supporting Variantsnssv3514988
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)nsv1052522
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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