A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259821



Internal ID20826861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:159751902..159752246hg38UCSC Ensembl
chr3:159469691..159470035hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560457
Supporting Variants
Samples
Known GenesIQCJ-SCHIP1, SCHIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259821
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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