A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511094



Internal ID20884419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77860001..78004300hg38UCSC Ensembl
chr15:78152343..78296642hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38144300
hg19144300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2597n223
Supporting Variantsnssv18183136
Samples
Known GenesLOC645752, LOC91450, TBC1D2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511094
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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