A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429960



Internal ID21087513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:83517695..83518111hg38UCSC Ensembl
chr8:84429930..84430346hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38417
hg19417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18172946
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429960
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