A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417258



Internal ID21074811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3137961..3274613hg38UCSC Ensembl
chr9:3137961..3274613hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38136653
hg19136653
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221067
Samples
Known GenesRFX3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417258
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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