A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026395



Internal ID20593435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71432501..71433300hg38UCSC Ensembl
chr15:71724840..71725639hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514572
Supporting Variants
Samples
Known GenesTHSD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026395
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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