A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598616



Internal ID20971687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37618001..37619274hg38UCSC Ensembl
chr22:38014008..38015281hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg381274
hg191274
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254945
Samples
Known GenesGGA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598616
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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