A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17030979



Internal ID88353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1473233..1477641hg38UCSC Ensembl
chr10:1515428..1519836hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg384409
hg194409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5479839
Supporting Variants
Samples
Known GenesADARB2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17030979
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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