A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17435013



Internal ID22492883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102842426..102842493hg38UCSC Ensembl
chr8:103854654..103854721hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5925074
Supporting Variants
Samples
Known GenesAZIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17435013
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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