A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038207



Internal ID93200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:84716289..84716597hg38UCSC Ensembl
chr10:86476045..86476353hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5493455
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038207
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.02123


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