A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703890



Internal ID127556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68199818..68200164hg38UCSC Ensembl
chr15:68492156..68492502hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521677
Supporting Variants
Samples
Known GenesCALML4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703890
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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