A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6144293



Internal ID343497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70541046..70541149hg38UCSC Ensembl
chr15:70833385..70833488hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702340
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6144293
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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