A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17013529



Internal ID76693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90090357..90095500hg38UCSC Ensembl
chr8:91102585..91107728hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg385144
hg195144
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147095
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17013529
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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