A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3514988



Internal ID18813269
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 StatusS
Merged Variantsnsv1052522
Supporting Variants
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)nssv3514988
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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