A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247006



Internal ID20814046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13690777..13691222hg38UCSC Ensembl
chr1:14017272..14017717hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38446
hg19446
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550944
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247006
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00018


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