A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440398



Internal ID21097951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83976401..83984900hg38UCSC Ensembl
chr9:86591316..86599815hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg388500
hg198500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230946
Samples
Known GenesHNRNPK, RMI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440398
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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