A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249002



Internal ID20816042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244663394..244663822hg38UCSC Ensembl
chr1:244826696..244827124hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38429
hg19429
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546217
Supporting Variants
Samples
Known GenesDESI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249002
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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