A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv764533



Internal ID16058489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2428341..2429689hg38UCSC Ensembl
Innerchr11:2449571..2450919hg19UCSC Ensembl
Innerchr11:2406147..2407495hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg381349
hg191349
hg181349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553103
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv764533
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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