A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17510314



Internal ID22568264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98393716..98413228hg38UCSC Ensembl
chr8:99405944..99425456hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg3819513
hg1919513
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852093
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17510314
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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