A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558614



Internal ID20931685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:122892600..122893903hg38UCSC Ensembl
chr5:122228295..122229598hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg381304
hg191304
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266219
Samples
Known GenesSNX24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558614
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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