A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940293



Internal ID22715700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26167841..26171357hg38UCSC Ensembl
chr18:23747805..23751321hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg383517
hg193517
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17370210
Samples
Known GenesPSMA8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940293
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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