A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142422



Internal ID341622
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 StatusM
Merged Variants
Supporting Variantsnssv17029439
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142422
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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