A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18167457



Internal ID20734497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:36211041..36211542hg38UCSC Ensembl
chr8:36068559..36069060hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6420804
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18167457
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00045


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