A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433159



Internal ID21090712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100364423..100365410hg38UCSC Ensembl
chr8:101376651..101377638hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg38988
hg19988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161345
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433159
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