A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196823



Internal ID20763863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51932166..52011423hg38UCSC Ensembl
chr15:52224363..52303620hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3879258
hg1979258
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505222
Supporting Variants
Samples
Known GenesLEO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196823
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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