A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249363



Internal ID20816403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:224255341..224256215hg38UCSC Ensembl
chr1:224443043..224443917hg19UCSC Ensembl
Cytoband1q42.11
Allele length
AssemblyAllele length
hg38875
hg19875
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537663
Supporting Variants
Samples
Known GenesNVL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249363
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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