A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173553



Internal ID20740593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97695965..97696353hg38UCSC Ensembl
chr8:98708193..98708581hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38389
hg19389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424187
Supporting Variants
Samples
Known GenesMTDH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173553
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