A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553088



Internal ID15993811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2377616..2397200hg38UCSC Ensembl
Innerchr11:2398846..2418430hg19UCSC Ensembl
Innerchr11:2355422..2375006hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3819585
hg1919585
hg1819585
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1568n54
Supporting Variantsnssv764509
Samples
Known GenesCD81, CD81-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553088
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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