A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17018475



Internal ID79953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144799801..144835343hg38UCSC Ensembl
chr8:146025186..146060728hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3835543
hg1935543
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147331
Supporting Variants
Samples
Known GenesZNF517, ZNF7
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17018475
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.001561


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