A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563243



Internal ID20936314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:79466964..79467202hg38UCSC Ensembl
chr5:78762787..78763025hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270302
Samples
Known GenesHOMER1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563243
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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