A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496789



Internal ID20869992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68535639..68542379hg38UCSC Ensembl
chr15:68827978..68834718hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg386741
hg196741
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191856
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496789
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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