A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553986



Internal ID15994709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31467343..31657500hg38UCSC Ensembl
Innerchr11:31488890..31679048hg19UCSC Ensembl
Innerchr11:31445466..31635624hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38190158
hg19190159
hg18190159
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1740n54
Supporting Variantsnssv771045, nssv771044
Samples
Known GenesELP4, IMMP1L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553986
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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