A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146117



Internal ID345322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28462874..28602874hg38UCSC Ensembl
chr15:28708020..28848020hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38140001
hg19140001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17699605
Samples
Known GenesGOLGA8F, GOLGA8G, MIR4509-1, MIR4509-2, MIR4509-3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146117
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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