A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192242



Internal ID20759282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76859326..76871911hg38UCSC Ensembl
chr14:77325669..77338254hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3812586
hg1912586
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6484783
Supporting Variants
Samples
Known GenesC14orf166B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192242
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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