A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426808



Internal ID21084361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54637978..54683951hg38UCSC Ensembl
chr8:55550538..55596511hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3845974
hg1945974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169069
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426808
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