A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181663



Internal ID20748703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77590389..77624773hg38UCSC Ensembl
chr15:77882731..77917115hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3834385
hg1934385
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514513
Supporting Variants
Samples
Known GenesLINGO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181663
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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