A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515250



Internal ID20888609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69645469..69649096hg38UCSC Ensembl
chr15:69937808..69941435hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383628
hg193628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026317
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515250
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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