A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190692



Internal ID20757732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103730346..103733709hg38UCSC Ensembl
chr14:104196683..104200046hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg383364
hg193364
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514845
Supporting Variants
Samples
Known GenesZFYVE21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190692
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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