A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184303



Internal ID20751343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73364287..73371400hg38UCSC Ensembl
chr14:73830995..73838108hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg387114
hg197114
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6489534
Supporting Variants
Samples
Known GenesNUMB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184303
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00059


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