A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv777177



Internal ID15724447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:65535422..65540385hg38UCSC Ensembl
Innerchr11:65302893..65307856hg19UCSC Ensembl
Innerchr11:65059469..65064432hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg384964
hg194964
hg184964
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555212
Supporting Variants
Samples
Known GenesLTBP3, SCYL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv777177
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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