A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035830



Internal ID91634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59627367..59627532hg38UCSC Ensembl
chr10:61387125..61387290hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5475805
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035830
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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