A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193093



Internal ID20760133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51882701..51885400hg38UCSC Ensembl
chr15:52174898..52177597hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503297
Supporting Variants
Samples
Known GenesTMOD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193093
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00084


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