A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590131



Internal ID20963202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58327741..58328759hg38UCSC Ensembl
chr14:58794459..58795477hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg381019
hg191019
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237892
Samples
Known GenesARID4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590131
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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