A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17100809



Internal ID21412165
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 StatusS
Merged Variantsnsv5596507
Supporting Variants
SamplesHG00513
Known GenesPSMA8
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17100809
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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