A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249444



Internal ID20816484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:226236462..226237546hg38UCSC Ensembl
chr1:226424163..226425247hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg381085
hg191085
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550326
Supporting Variants
Samples
Known GenesLIN9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249444
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00018


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