A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188184



Internal ID20755224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100301007..100315760hg38UCSC Ensembl
chr14:100767344..100782097hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3814754
hg1914754
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510815
Supporting Variants
Samples
Known GenesMIR345, SLC25A29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188184
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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