A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225081



Internal ID20792121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:103902601..103941000hg38UCSC Ensembl
chr8:104914829..104953228hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3838400
hg1938400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6431530
Supporting Variants
Samples
Known GenesRIMS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225081
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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