A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17519337



Internal ID21843696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:218894010..218898375hg38UCSC Ensembl
chr2:219758732..219763097hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg384366
hg194366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5988143
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17519337
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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