A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185022



Internal ID20752062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51509315..51572169hg38UCSC Ensembl
chr15:51801512..51864366hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3862855
hg1962855
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501849
Supporting Variants
Samples
Known GenesDMXL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185022
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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