A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234756



Internal ID20801796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:122257235..122276075hg38UCSC Ensembl
chr9:125019514..125038354hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3818841
hg1918841
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436334
Supporting Variants
Samples
Known GenesMRRF, RBM18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234756
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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