A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247332



Internal ID20814372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16081191..16082268hg38UCSC Ensembl
chr1:16407686..16408763hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg381078
hg191078
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540184
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247332
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.01998


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