A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510354



Internal ID20883672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25636101..25649259hg38UCSC Ensembl
chr15:25881248..25894406hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3813159
hg1913159
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179837
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510354
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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