A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594668



Internal ID20967739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:54289735..54434275hg38UCSC Ensembl
chr14:54756453..54900993hg19UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg38144541
hg19144541
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237768
Samples
Known GenesCDKN3, CNIH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594668
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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