A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155893



Internal ID22086398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:183880234..183985159hg38UCSC Ensembl
Outerchr2:183875007..183987069hg38UCSC Ensembl
Innerchr2:184744961..184849886hg19UCSC Ensembl
Outerchr2:184739734..184851796hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38112063
hg19112063
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016124
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155893
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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