A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920839



Internal ID22696062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:118113599..118113770hg38UCSC Ensembl
chr8:119125838..119126009hg19UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442332
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920839
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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