A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236805



Internal ID20803845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102200979..102319280hg38UCSC Ensembl
chr8:103213207..103331508hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38118302
hg19118302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429240
Supporting Variants
Samples
Known GenesRRM2B, UBR5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236805
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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