A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17015602



Internal ID78052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:91792348..91797993hg38UCSC Ensembl
chr8:92804576..92810221hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg385646
hg195646
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476342
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17015602
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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