A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17000890



Internal ID68156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106175564..106179811hg38UCSC Ensembl
chr7:105816010..105820257hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg384248
hg194248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488281
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17000890
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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