A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232664



Internal ID20799704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22323319..22324044hg38UCSC Ensembl
chr10:22612248..22612973hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg38726
hg19726
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587851
Supporting Variants
Samples
Known GenesBMI1, COMMD3-BMI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232664
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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