A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506496



Internal ID20879777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69455999..69478943hg38UCSC Ensembl
chr15:69748338..69771282hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3822945
hg1922945
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192367
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506496
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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