A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508498



Internal ID20881800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69821913..69825277hg38UCSC Ensembl
chr15:70114252..70117616hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383365
hg193365
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182365
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508498
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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