A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16996202



Internal ID64918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38071930..38073642hg38UCSC Ensembl
chr7:38111532..38113244hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg381713
hg191713
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559590
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16996202
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.058713


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