A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155286



Internal ID22085791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:35593868..35742970hg38UCSC Ensembl
Outerchr2:35590727..35750907hg38UCSC Ensembl
Innerchr2:35818934..35968036hg19UCSC Ensembl
Outerchr2:35815793..35975973hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38160181
hg19160181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4007643
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155286
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer