A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155164



Internal ID22085669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:11010252..11013945hg38UCSC Ensembl
Outerchr2:11007859..11014144hg38UCSC Ensembl
Innerchr2:11150378..11154071hg19UCSC Ensembl
Outerchr2:11147985..11154270hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg386286
hg196286
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4007591
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155164
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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