A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4005753



Internal ID22067384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11827328..11877531hg38UCSC Ensembl
Outerchr11:11827028..11881297hg38UCSC Ensembl
Innerchr11:11848875..11899078hg19UCSC Ensembl
Outerchr11:11848575..11902844hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3854270
hg1954270
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154695
Supporting Variants
Samples
Known GenesUSP47
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4005753
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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