A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17013364



Internal ID76581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80629070..80629121hg38UCSC Ensembl
chr8:81541305..81541356hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5405543
Supporting Variants
Samples
Known GenesZNF704
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17013364
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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