A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508852



Internal ID20882156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62210394..62215244hg38UCSC Ensembl
chr15:62502593..62507443hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg384851
hg194851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025575
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508852
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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