A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491302



Internal ID21148855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23639903..23659521hg38UCSC Ensembl
chr14:24109112..24128730hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3819619
hg1919619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016745
Samples
Known GenesDHRS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491302
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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