A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv764466



Internal ID16058422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1753904..1785884hg38UCSC Ensembl
Innerchr11:1775134..1807114hg19UCSC Ensembl
Innerchr11:1731710..1763690hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3831981
hg1931981
hg1831981
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553049
Supporting Variants
Samples
Known GenesCTSD, MOB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv764466
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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