A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593171



Internal ID20966242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73672434..73672927hg38UCSC Ensembl
chr14:74139137..74139630hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38494
hg19494
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238684
Samples
Known GenesDNAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593171
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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