A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155140



Internal ID22085645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:5744074..5764258hg38UCSC Ensembl
Outerchr2:5741052..5768019hg38UCSC Ensembl
Innerchr2:5884206..5904390hg19UCSC Ensembl
Outerchr2:5881184..5908151hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3826968
hg1926968
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4007586
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155140
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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