A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430524



Internal ID21088077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:19678576..19701399hg38UCSC Ensembl
chr8:19536087..19558910hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3822824
hg1922824
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165369
Samples
Known GenesCSGALNACT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430524
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