A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252741



Internal ID20819781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93104219..93104381hg38UCSC Ensembl
chr1:93569776..93569938hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537578
Supporting Variants
Samples
Known GenesMTF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252741
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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