A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503890



Internal ID20877148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:87127901..87133400hg38UCSC Ensembl
chr15:87671132..87676631hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180240
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503890
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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