A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247763



Internal ID20814803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157391203..157400396hg38UCSC Ensembl
chr1:157360993..157370186hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg389194
hg199194
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542763
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247763
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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