A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033639



Internal ID21942982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26165033..26165985hg38UCSC Ensembl
chr18:23744997..23745949hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38953
hg19953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621150
Samples
Known GenesPSMA8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033639
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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