A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910826



Internal ID22686038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42714289..42718480hg38UCSC Ensembl
chr8:42569432..42573623hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg384192
hg194192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2008n209
Supporting Variantsnssv17445461
Samples
Known GenesCHRNB3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910826
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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