A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429682



Internal ID21087235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:110255984..110270554hg38UCSC Ensembl
chr8:111268213..111282783hg19UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg3814571
hg1914571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162577
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429682
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