A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196442



Internal ID20763482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:42428220..43069422hg38UCSC Ensembl
chr14:42897423..43538625hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38641203
hg19641203
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6488306
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196442
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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