A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236842



Internal ID20803882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:135004080..135812098hg38UCSC Ensembl
chr8:136016323..136824341hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38808019
hg19808019
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6423173
Supporting Variants
Samples
Known GenesKHDRBS3, LOC286094
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236842
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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