A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591279



Internal ID20964350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:50526544..50527023hg38UCSC Ensembl
chr14:50993262..50993741hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38480
hg19480
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2155n223
Supporting Variantsnssv18220208
Samples
Known GenesMAP4K5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591279
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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