A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581348



Internal ID20954419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103673647..103674517hg38UCSC Ensembl
chr14:104139984..104140854hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38871
hg19871
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237091
Samples
Known GenesKLC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581348
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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