A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18165081



Internal ID20732121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:13039942..13055160hg38UCSC Ensembl
chr8:12897451..12912669hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3815219
hg1915219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6428242
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18165081
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