A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv768989



Internal ID15716259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:24413656..24516078hg38UCSC Ensembl
Innerchr11:24435202..24537624hg19UCSC Ensembl
Innerchr11:24391778..24494200hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38102423
hg19102423
hg18102423
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553794
Supporting Variants
Samples
Known GenesLUZP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv768989
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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