A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228133



Internal ID20795173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10205320..10652322hg38UCSC Ensembl
chr8:10062830..10509832hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38447003
hg19447003
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6419536
Supporting Variants
Samples
Known GenesMSRA, PRSS55, RP1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228133
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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