A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182850



Internal ID20749890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50146101..50195900hg38UCSC Ensembl
chr15:50438298..50488097hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3849800
hg1949800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504360
Supporting Variants
Samples
Known GenesSLC27A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182850
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00071


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