A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17685503



Internal ID109169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:131164987..131493164hg38UCSC Ensembl
chr12:131649532..131977709hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38328178
hg19328178
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556837
Supporting Variants
Samples
Known GenesLOC116437, LOC338797
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17685503
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.083359


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