A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506742



Internal ID20880026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58594801..58596900hg38UCSC Ensembl
chr15:58887000..58889099hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026178
Samples
Known GenesADAM10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506742
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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