A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182084



Internal ID20749124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94856110..94870767hg38UCSC Ensembl
chr14:95322447..95337104hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3814658
hg1914658
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501641
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182084
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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