A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517701



Internal ID21842060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:208508527..208548001hg38UCSC Ensembl
chr2:209373252..209412726hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3839475
hg1939475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5987420
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17517701
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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