A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559573



Internal ID20932644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:119603169..120129169hg38UCSC Ensembl
chr5:118938864..119464864hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38526001
hg19526001
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266179
Samples
Known GenesFAM170A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559573
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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