A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145734



Internal ID344939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74020000..74088987hg38UCSC Ensembl
chr15:74312341..74381328hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3868988
hg1968988
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701055
Samples
Known GenesGOLGA6A, PML
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145734
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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