A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250424



Internal ID20817464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58679606..58681118hg38UCSC Ensembl
chr1:59145278..59146790hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg381513
hg191513
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6538246
Supporting Variants
Samples
Known GenesMYSM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250424
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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