A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908280



Internal ID22683490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:133033312..133033365hg38UCSC Ensembl
chr8:134045557..134045610hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444578
Samples
Known GenesTG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908280
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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