A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4006739



Internal ID22068370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:27808429..27882134hg38UCSC Ensembl
Outerchr11:27801732..27884989hg38UCSC Ensembl
Innerchr11:27829976..27903681hg19UCSC Ensembl
Outerchr11:27823279..27906536hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3883258
hg1983258
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154710
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4006739
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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