A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140651



Internal ID339844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:75798082..75799640hg38UCSC Ensembl
chr5:75093907..75095465hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg381559
hg191559
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16967151
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140651
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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