A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247742



Internal ID20814782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156380107..156380694hg38UCSC Ensembl
chr1:156349898..156350485hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38588
hg19588
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540341
Supporting Variants
Samples
Known GenesRHBG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247742
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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