A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557269



Internal ID20930340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:53293620..53301643hg38UCSC Ensembl
chr5:52589450..52597473hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg388024
hg198024
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269047
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557269
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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