A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16983127



Internal ID56130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41110267..41110573hg38UCSC Ensembl
chr6:41078006..41078312hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559885
Supporting Variants
Samples
Known GenesADCY10P1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16983127
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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