A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4007242



Internal ID22068873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:92071139..92152402hg38UCSC Ensembl
Outerchr11:92070584..92156207hg38UCSC Ensembl
Innerchr11:91804305..91885568hg19UCSC Ensembl
Outerchr11:91803750..91889373hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3885624
hg1985624
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154760
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4007242
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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