A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17617236



Internal ID21809283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44539125..44547526hg38UCSC Ensembl
chr15:44831323..44839724hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg388402
hg198402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6032594
Supporting Variants
Samples
Known GenesEIF3J
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17617236
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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