A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703894



Internal ID127560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68244254..68247990hg38UCSC Ensembl
chr15:68536592..68540328hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383737
hg193737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521695
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703894
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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