A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254801



Internal ID20821841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:24860795..24861559hg38UCSC Ensembl
chr22:25256762..25257526hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38765
hg19765
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599457
Supporting Variants
Samples
Known GenesSGSM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254801
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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