A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038595



Internal ID93468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78897624..78907167hg38UCSC Ensembl
chr10:80657381..80666924hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg389544
hg199544
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5479140
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038595
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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