A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596639



Internal ID20969710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40629925..40630785hg38UCSC Ensembl
chr22:41025929..41026789hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38861
hg19861
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253806
Samples
Known GenesMKL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596639
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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