A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422017



Internal ID21079570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97077775..97104478hg38UCSC Ensembl
chr8:98090003..98116706hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3826704
hg1926704
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173510
Samples
Known GenesCPQ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422017
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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