A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597538



Internal ID20970609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45121830..45123509hg38UCSC Ensembl
chr22:45517711..45519390hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg381680
hg191680
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255069
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597538
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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