A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598563



Internal ID20971634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31770011..31770751hg38UCSC Ensembl
chr22:32165997..32166737hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38741
hg19741
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4687n223
Supporting Variantsnssv18255116
Samples
Known GenesDEPDC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598563
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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