A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491276



Internal ID21148829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58281658..58283371hg38UCSC Ensembl
chr14:58748376..58750089hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg381714
hg191714
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180012
Samples
Known GenesFLJ31306
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491276
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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