A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579790



Internal ID20952861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92030004..92030537hg38UCSC Ensembl
chr14:92496348..92496881hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg38534
hg19534
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237700
Samples
Known GenesTRIP11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579790
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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