A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506998



Internal ID20880286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53149045..53149513hg38UCSC Ensembl
chr15:53441242..53441710hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38469
hg19469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025959
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506998
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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