A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17434198



Internal ID22492068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11218819..11218924hg38UCSC Ensembl
chr8:11076328..11076433hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5920883
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17434198
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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