A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17037061



Internal ID92464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74781819..74794025hg38UCSC Ensembl
chr10:76541577..76553783hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3812207
hg1912207
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486824
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17037061
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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