A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249262



Internal ID20816302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:114742501..114743398hg38UCSC Ensembl
chr1:115285122..115286019hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38898
hg19898
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539855
Supporting Variants
Samples
Known GenesCSDE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249262
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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