A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596830



Internal ID20969901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:46213446..46215721hg38UCSC Ensembl
chr22:46609343..46611618hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg382276
hg192276
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4733n223
Supporting Variantsnssv18255674
Samples
Known GenesPPARA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596830
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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