A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17010142



Internal ID74396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28351218..28351328hg38UCSC Ensembl
chr8:28208735..28208845hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486690
Supporting Variants
Samples
Known GenesZNF395
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17010142
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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