A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196549



Internal ID20763589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51728201..51762100hg38UCSC Ensembl
chr15:52020398..52054297hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3833900
hg1933900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503279
Supporting Variants
Samples
Known GenesLYSMD2, TMOD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196549
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00048


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