A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563472



Internal ID20936543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:81406431..81406695hg38UCSC Ensembl
chr5:80702250..80702514hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38265
hg19265
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269004
Samples
Known GenesRNU5D-1, RNU5E-1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563472
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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