A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592107



Internal ID20965178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:63243340..63244587hg38UCSC Ensembl
chr14:63710058..63711305hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg381248
hg191248
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237203
Samples
Known GenesRHOJ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592107
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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