A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594060



Internal ID20967131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23287344..23287809hg38UCSC Ensembl
chr14:23756553..23757018hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38466
hg19466
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220164
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594060
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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