A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv778763



Internal ID16072719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:70130375..70137288hg38UCSC Ensembl
Innerchr11:69976481..69983394hg19UCSC Ensembl
Innerchr11:69654129..69661042hg18UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg386914
hg196914
hg186914
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555330
Supporting Variants
Samples
Known GenesANO1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv778763
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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