A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038657



Internal ID93515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79746368..79849368hg38UCSC Ensembl
chr10:81506124..81609124hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38103001
hg19103001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5483373
Supporting Variants
Samples
Known GenesLOC642361
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038657
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.011431


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