A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914830



Internal ID22690047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:127737925..127746763hg38UCSC Ensembl
chr8:128750171..128759009hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg388839
hg198839
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17438523
Samples
Known GenesMYC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914830
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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