A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454724



Internal ID21112277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134204749..134371412hg38UCSC Ensembl
chr9:137096595..137263258hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38166664
hg19166664
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232845
Samples
Known GenesRXRA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454724
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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