A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17053123



Internal ID103266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:11214148..11214277hg38UCSC Ensembl
chr12:11367049..11367178hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563504
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17053123
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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