A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17648842



Internal ID21840889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:315832..315884hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3853
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106458
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17648842
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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