A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251012



Internal ID20818052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:43718426..43719658hg38UCSC Ensembl
chr1:44184097..44185329hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg381233
hg191233
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545171
Supporting Variants
Samples
Known GenesST3GAL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251012
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00036


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