A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420534



Internal ID21078087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37005031..37005463hg38UCSC Ensembl
chr8:36862549..36862981hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38433
hg19433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168853
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420534
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