A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591777



Internal ID20964848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91148089..91148311hg38UCSC Ensembl
chr14:91614433..91614655hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237675
Samples
Known GenesC14orf159
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591777
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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