A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249921



Internal ID20816962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:12676677..12677326hg38UCSC Ensembl
chr1:12736688..12737337hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38650
hg19650
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540824
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249921
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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