A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147095



Internal ID346288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90090357..90095500hg38UCSC Ensembl
chr8:91102585..91107728hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg385144
hg195144
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17013529
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147095
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer