A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419263



Internal ID21076816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:127737925..127746764hg38UCSC Ensembl
chr8:128750171..128759010hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg388840
hg198840
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223281
Samples
Known GenesMYC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419263
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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