A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17004795



Internal ID70835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149156596..149157272hg38UCSC Ensembl
chr7:148853688..148854364hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38677
hg19677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5478403
Supporting Variants
Samples
Known GenesZNF398
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17004795
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001249


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