A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17029439



Internal ID87315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3818746..3830604hg38UCSC Ensembl
chr10:3860938..3872796hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3811859
hg1911859
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142422
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17029439
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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