A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556837



Internal ID329962
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 StatusM
Merged Variantsdgv115n206
Supporting Variantsnssv17685503
Samples
Known GenesLOC116437, LOC338797
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556837
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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