A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237669



Internal ID20804709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91050135..91050700hg38UCSC Ensembl
chr14:91516479..91517044hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38566
hg19566
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582042
Supporting Variants
Samples
Known GenesRPS6KA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237669
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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