A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145135



Internal ID344340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28354874..28452874hg38UCSC Ensembl
chr15:28600020..28698020hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3898001
hg1998001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17699599
Samples
Known GenesGOLGA8F, GOLGA8G, MIR4509-1, MIR4509-2, MIR4509-3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145135
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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