A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580527



Internal ID20953598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55378816..55379561hg38UCSC Ensembl
chr14:55845534..55846279hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38746
hg19746
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2162n223
Supporting Variantsnssv18237821
Samples
Known GenesATG14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580527
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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