A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17506219



Internal ID22564165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:125777233..125785280hg38UCSC Ensembl
chr8:126789477..126797524hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg388048
hg198048
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856806
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17506219
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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