A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155855



Internal ID22086360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:122083944..122152955hg38UCSC Ensembl
Outerchr2:122078865..122162999hg38UCSC Ensembl
Innerchr2:122841520..122910531hg19UCSC Ensembl
Outerchr2:122836441..122920575hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg3884135
hg1984135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4013300
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155855
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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