A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598696



Internal ID20971767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11549732..11556767hg38UCSC Ensembl
chrUn_gl000232:2395..9430hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg387036
hg197036
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254273
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598696
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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