A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249005



Internal ID20816045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244702326..244703004hg38UCSC Ensembl
chr1:244865628..244866306hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38679
hg19679
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551871
Supporting Variants
Samples
Known GenesDESI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249005
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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