A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252387



Internal ID20819427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31047989..31048719hg38UCSC Ensembl
chr1:31520836..31521566hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542931
Supporting Variants
Samples
Known GenesPUM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252387
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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