A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249219



Internal ID20816259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:101414563..101426265hg38UCSC Ensembl
chr1:101880119..101891821hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg3811703
hg1911703
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544529
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249219
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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