A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv764507



Internal ID15711777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2300156..2304351hg38UCSC Ensembl
Innerchr11:2321386..2325581hg19UCSC Ensembl
Innerchr11:2277962..2282157hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg384196
hg194196
hg184196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553086
Supporting Variants
Samples
Known GenesC11orf21, TSPAN32
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv764507
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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