A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044622



Internal ID19133841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:101791468..101818580hg38UCSC Ensembl
Innerchr11:101662199..101689311hg19UCSC Ensembl
Innerchr11:101167409..101194521hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3827113
hg1927113
hg1827113
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3516307
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)nsv1044622
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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