A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6144833



Internal ID344038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:93138661..93152264hg38UCSC Ensembl
chr15:93681890..93695493hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3813604
hg1913604
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17703730
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6144833
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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