A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18164089



Internal ID20731129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:115668101..115669200hg38UCSC Ensembl
chr8:116680328..116681427hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6419262
Supporting Variants
Samples
Known GenesTRPS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18164089
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.09917


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