A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592361



Internal ID20965432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39042416..39137637hg38UCSC Ensembl
chr14:39511620..39606841hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3895222
hg1995222
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228636
Samples
Known GenesGEMIN2, SEC23A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592361
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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