A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17735583



Internal ID159249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:84793660..84793847hg38UCSC Ensembl
chr6:85503378..85503565hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38188
hg19188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5473299
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17735583
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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