A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711012



Internal ID134678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:4866112..4876882hg38UCSC Ensembl
chr17:4769407..4780177hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3810771
hg1910771
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563101
Supporting Variants
Samples
Known GenesMINK1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711012
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer