A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17055865



Internal ID105076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:11467018..12059240hg38UCSC Ensembl
chr12:11619952..12212174hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38592223
hg19592223
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556193
Supporting Variants
Samples
Known GenesETV6, LOC338817, RNU6-19P
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17055865
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


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