A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251166



Internal ID20818206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47390396..47391495hg38UCSC Ensembl
chr1:47856068..47857167hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544614
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251166
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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