A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18164937



Internal ID20731977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:126637468..126652262hg38UCSC Ensembl
chr8:127649713..127664507hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3814795
hg1914795
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415706
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18164937
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