A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583293



Internal ID20956364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73914829..73915105hg38UCSC Ensembl
chr14:74381532..74381808hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238703
Samples
Known GenesZNF410
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583293
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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