A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880356



Internal ID22655326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:104929098..104933614hg38UCSC Ensembl
chr2:105545556..105550072hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg384517
hg194517
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399181
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880356
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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