A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248009



Internal ID20815049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165770121..165771276hg38UCSC Ensembl
chr1:165739358..165740513hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg381156
hg191156
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539985
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248009
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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