A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145421



Internal ID344626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:93259793..93279373hg38UCSC Ensembl
chr15:93803022..93822602hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3819581
hg1919581
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17703741
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145421
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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