A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155919



Internal ID22086424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:215611315..215656737hg38UCSC Ensembl
Outerchr2:215607975..215661288hg38UCSC Ensembl
Innerchr2:216476038..216521460hg19UCSC Ensembl
Outerchr2:216472698..216526011hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3853314
hg1953314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016184
Samples
Known GenesLINC00607
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155919
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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