A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv778757



Internal ID16072713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:69166429..69261081hg38UCSC Ensembl
Innerchr11:68933897..69028548hg19UCSC Ensembl
Innerchr11:68690473..68785124hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3894653
hg1994652
hg1894652
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555319
Supporting Variants
Samples
Known GenesLOC338694
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv778757
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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