A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184064



Internal ID20751104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71321187..71324186hg38UCSC Ensembl
chr14:71787904..71790903hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6483603
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184064
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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