A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17002859



Internal ID69524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98411601..98414647hg38UCSC Ensembl
chr7:98040913..98043959hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg383047
hg193047
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474743
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17002859
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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