A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249356



Internal ID20816396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:224209631..224210903hg38UCSC Ensembl
chr1:224397333..224398605hg19UCSC Ensembl
Cytoband1q42.11
Allele length
AssemblyAllele length
hg381273
hg191273
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552832
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249356
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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