A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147094



Internal ID346287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:66141241..66146606hg38UCSC Ensembl
chr13:66715373..66720738hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg385366
hg195366
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17692099
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147094
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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