A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv764281



Internal ID15711551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1412139..1417671hg38UCSC Ensembl
Innerchr11:1433369..1438901hg19UCSC Ensembl
Innerchr11:1389945..1395477hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg385533
hg195533
hg185533
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552985
Supporting Variants
Samples
Known GenesBRSK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv764281
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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