A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041652



Internal ID18784183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131842569..131874253hg38UCSC Ensembl
Innerchr11:131712463..131744147hg19UCSC Ensembl
Innerchr11:131217673..131249357hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3831685
hg1931685
hg1831685
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1299n100
Supporting Variantsnssv3513286
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)nsv1041652
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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