A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434628



Internal ID21092181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33306401..33310600hg38UCSC Ensembl
chr8:33163919..33168118hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166618
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434628
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