A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552758



Internal ID16340167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:174837..196533hg38UCSC Ensembl
Innerchr11:174837..196533hg19UCSC Ensembl
Innerchr11:164837..186533hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3821697
hg1921697
hg1821697
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1504n54
Supporting Variantsnssv763033
Samples
Known GenesLOC653486, SCGB1C1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552758
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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