A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147132



Internal ID343273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86742180..86747434hg38UCSC Ensembl
chr16:86775786..86781040hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg385255
hg195255
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17708414
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147132
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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