A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17018417



Internal ID79907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:143003113..143012251hg38UCSC Ensembl
chr8:144084530..144093668hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg389139
hg199139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476672
Supporting Variants
Samples
Known GenesLOC100133669
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17018417
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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