A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17438938



Internal ID22496808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93161565..93166130hg38UCSC Ensembl
chr8:94173794..94178359hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg384566
hg194566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5915503
Supporting Variants
Samples
Known GenesC8orf87
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17438938
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