A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515260



Internal ID20888619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41171616..41173836hg38UCSC Ensembl
chr15:41463814..41466034hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg382221
hg192221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023653
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515260
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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