A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182313



Internal ID20749353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22894456..22895099hg38UCSC Ensembl
chr14:23363665..23364308hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38644
hg19644
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6479073
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182313
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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