A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17598706



Internal ID21790751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53417886..53421843hg38UCSC Ensembl
chr15:53710083..53714040hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg383958
hg193958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6022499
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17598706
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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