A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019594



Internal ID21928937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37927561..37927637hg38UCSC Ensembl
chr8:37785079..37785155hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562385
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019594
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer