A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039574



Internal ID20606614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26182101..26186200hg38UCSC Ensembl
chr18:23762065..23766164hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533151
Supporting Variants
Samples
Known GenesPSMA8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039574
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.03174


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