A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711747



Internal ID135413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15962066..16010762hg38UCSC Ensembl
chr17:15865380..15914076hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3848697
hg1948697
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555899
Supporting Variants
Samples
Known GenesADORA2B, TTC19, ZSWIM7
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711747
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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