A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17058754



Internal ID107031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:52203845..52203855hg38UCSC Ensembl
chr12:52597629..52597639hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg3811
hg1911
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557927
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17058754
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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