A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250002



Internal ID20817042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206767001..206767762hg38UCSC Ensembl
chr1:206940346..206941107hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38762
hg19762
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542614
Supporting Variants
Samples
Known GenesIL10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250002
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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