A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920341



Internal ID22695564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54022904..54027883hg38UCSC Ensembl
chr8:54935464..54940443hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg384980
hg194980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448621
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920341
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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