A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17700876



Internal ID124542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58043836..58052956hg38UCSC Ensembl
chr15:58336034..58345154hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg389121
hg199121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5527738
Supporting Variants
Samples
Known GenesALDH1A2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17700876
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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