A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485090



Internal ID21142643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75575659..75594803hg38UCSC Ensembl
chr14:76042002..76061146hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3819145
hg1919145
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189097
Samples
Known GenesFLVCR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485090
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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