A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044874



Internal ID18787405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131856952..131874253hg38UCSC Ensembl
Innerchr11:131726846..131744147hg19UCSC Ensembl
Innerchr11:131232056..131249357hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3817302
hg1917302
hg1817302
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3511377
Samples
Known GenesNTM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044874
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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