A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599450



Internal ID20972521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:28974035..28975207hg38UCSC Ensembl
chr22:29370023..29371195hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg381173
hg191173
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4676n223
Supporting Variantsnssv18255482
Samples
Known GenesZNRF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599450
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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