A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552756



Internal ID16340165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:173466..196425hg38UCSC Ensembl
Innerchr11:173466..196425hg19UCSC Ensembl
Innerchr11:163466..186425hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3822960
hg1922960
hg1822960
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1504n54
Supporting Variantsnssv763031
Samples
Known GenesLOC653486, SCGB1C1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552756
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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