A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252746



Internal ID20819786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93163523..93163972hg38UCSC Ensembl
chr1:93629080..93629529hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551293
Supporting Variants
Samples
Known GenesTMED5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252746
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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