A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183183



Internal ID20750223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73301967..73320117hg38UCSC Ensembl
chr14:73768675..73786825hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3818151
hg1918151
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477743
Supporting Variants
Samples
Known GenesNUMB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183183
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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