A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185783



Internal ID20752823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75092239..75102619hg38UCSC Ensembl
chr14:75558942..75569322hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3810381
hg1910381
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6483549
Supporting Variants
Samples
Known GenesNEK9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185783
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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