A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17537497



Internal ID21861852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:69653932..69658746hg38UCSC Ensembl
chr2:69881064..69885878hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg384815
hg194815
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5989808
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17537497
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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