A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17057480



Internal ID106165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:33091853..33097520hg38UCSC Ensembl
chr12:33244787..33250454hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg385668
hg195668
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556212
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17057480
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000781


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