A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582980



Internal ID20956051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55407550..55407661hg38UCSC Ensembl
chr14:55874268..55874379hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237826
Samples
Known GenesATG14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582980
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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