A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584348



Internal ID20957419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103387784..103389734hg38UCSC Ensembl
chr14:103854121..103856071hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg381951
hg191951
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224096
Samples
Known GenesMARK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584348
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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