A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049802



Internal ID18792333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:22813787..23248080hg38UCSC Ensembl
Innerchr11:22835333..23269626hg19UCSC Ensembl
Innerchr11:22791909..23226202hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38434294
hg19434294
hg18434294
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3512260
Samples
Known GenesCCDC179, SVIP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049802
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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