A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595856



Internal ID20968927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:34273504..34274730hg38UCSC Ensembl
chr22:34669494..34670720hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg381227
hg191227
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4692n223
Supporting Variantsnssv18255178
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595856
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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