A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155918



Internal ID22086423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:215251325..215291712hg38UCSC Ensembl
Outerchr2:215241053..215294486hg38UCSC Ensembl
Innerchr2:216116048..216156435hg19UCSC Ensembl
Outerchr2:216105776..216159209hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3853434
hg1953434
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016183
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155918
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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