A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509306



Internal ID20882615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:94130201..94133200hg38UCSC Ensembl
chr15:94673430..94676429hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027030
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509306
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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