A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17016852



Internal ID78894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:112129806..112142520hg38UCSC Ensembl
chr8:113142035..113154749hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3812715
hg1912715
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480432
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17016852
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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