A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510682



Internal ID20884003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69975349..69977138hg38UCSC Ensembl
chr15:70267688..70269477hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381790
hg191790
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179211
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510682
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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