A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17054208



Internal ID103967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:13587176..13587288hg38UCSC Ensembl
chr12:13740110..13740222hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557289
Supporting Variants
Samples
Known GenesGRIN2B
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17054208
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


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