A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427753



Internal ID21085306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:117106677..117107123hg38UCSC Ensembl
chr8:118118916..118119362hg19UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg38447
hg19447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18163744
Samples
Known GenesSLC30A8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427753
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