A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155933



Internal ID22086438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:241973315..242078958hg38UCSC Ensembl
Outerchr2:241841244..242081572hg38UCSC Ensembl
Innerchr2:242915466..243021109hg19UCSC Ensembl
Outerchr2:242783396..243023723hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38240329
hg19240328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv177n97
Supporting Variantsnssv4016203
Samples
Known GenesCXXC11, PDCD1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155933
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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