A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455507



Internal ID233586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10023937..10024049hg38UCSC Ensembl
chr6:10024170..10024282hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979520
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455507
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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