A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17433114



Internal ID22490984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:137616910..137638395hg38UCSC Ensembl
chr8:138629153..138650638hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3821486
hg1921486
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5908503
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17433114
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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