A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18170367



Internal ID20737407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73441901..73444200hg38UCSC Ensembl
chr8:74354136..74356435hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429443
Supporting Variants
Samples
Known GenesSTAU2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18170367
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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