A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18162733



Internal ID20729773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:104511306..104512262hg38UCSC Ensembl
chr8:105523534..105524490hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38957
hg19957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422425
Supporting Variants
Samples
Known GenesLRP12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18162733
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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