A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3519944



Internal ID18818225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:86698017..86793113hg38UCSC Ensembl
Innerchr11:86409059..86504155hg19UCSC Ensembl
Innerchr11:86086707..86181803hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3895097
hg1995097
hg1895097
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049157
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)nssv3519944
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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