A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18246905



Internal ID20813946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:47167313..47168078hg38UCSC Ensembl
chr18:44693684..44694449hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg38766
hg19766
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585522
Supporting Variants
Samples
Known GenesIER3IP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18246905
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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