A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917279



Internal ID22692498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:133777332..133777490hg38UCSC Ensembl
chr8:134789575..134789733hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447736
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917279
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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