A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597445



Internal ID20970516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:43929411..43929726hg38UCSC Ensembl
chr22:44325291..44325606hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255052
Samples
Known GenesPNPLA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597445
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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