A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189145



Internal ID20756185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92137201..92140600hg38UCSC Ensembl
chr15:92680431..92683830hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg383400
hg193400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496196
Supporting Variants
Samples
Known GenesSLCO3A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189145
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00151


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