A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436334



Internal ID21093887
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 StatusM
Merged Variants
Supporting Variantsnssv18234756
Samples
Known GenesMRRF, RBM18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436334
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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