A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17058659



Internal ID106968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:53306612..53307373hg38UCSC Ensembl
chr12:53700396..53701157hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38762
hg19762
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555255
Supporting Variants
Samples
Known GenesC12orf10
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17058659
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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