A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196341



Internal ID20763381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:62117702..62146583hg38UCSC Ensembl
chr14:62584420..62613301hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3828882
hg1928882
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6492187
Supporting Variants
Samples
Known GenesLINC00643, LINC00644
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196341
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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