A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247004



Internal ID20814044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13670678..13672020hg38UCSC Ensembl
chr1:13997173..13998515hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg381343
hg191343
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546515
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247004
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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