A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505495



Internal ID20878765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70524544..70545155hg38UCSC Ensembl
chr15:70816883..70837494hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3820612
hg1920612
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180265
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505495
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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