A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16948108



Internal ID32769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40233406..40235438hg38UCSC Ensembl
chr4:40235026..40237058hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg382033
hg192033
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557003
Supporting Variants
Samples
Known GenesRHOH
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16948108
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.177233


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