A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155864



Internal ID22086369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:129231356..129782082hg38UCSC Ensembl
Outerchr2:129229318..129783197hg38UCSC Ensembl
Innerchr2:129988929..130539655hg19UCSC Ensembl
Outerchr2:129986891..130540770hg19UCSC Ensembl
Cytoband2q21.1
Allele length
AssemblyAllele length
hg38553880
hg19553880
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4014416
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155864
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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