A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17710927



Internal ID134593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:2429898..2512511hg38UCSC Ensembl
chr17:2333192..2415805hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3882614
hg1982614
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147057
Supporting Variants
Samples
Known GenesMETTL16
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17710927
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.019513


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