A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4007324



Internal ID22068955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:127784065..127870165hg38UCSC Ensembl
Outerchr11:127776182..127873455hg38UCSC Ensembl
Innerchr11:127653960..127740060hg19UCSC Ensembl
Outerchr11:127646077..127743350hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3897274
hg1997274
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154782
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4007324
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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