A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496080



Internal ID20869278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69065055..69110341hg38UCSC Ensembl
chr15:69357395..69402681hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3845287
hg1945287
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196342
Samples
Known GenesLINC00277, MIR548H4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496080
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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