A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17014768



Internal ID77509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101317672..101317748hg38UCSC Ensembl
chr8:102329900..102329976hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141556
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17014768
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003282


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