A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221354



Internal ID20788394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:70402651..70403328hg38UCSC Ensembl
chr12:70796431..70797108hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg38678
hg19678
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589608
Supporting Variants
Samples
Known GenesKCNMB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221354
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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