A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515362



Internal ID20888721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:94279940..94295773hg38UCSC Ensembl
chr15:94823169..94839002hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3815834
hg1915834
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027044
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515362
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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