A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145066



Internal ID344271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72460697..72460768hg38UCSC Ensembl
chr15:72753038..72753109hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702440
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145066
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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