A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555019



Internal ID328187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15782634..15788701hg38UCSC Ensembl
chr9:15782632..15788699hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg386068
hg196068
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17021579
Samples
Known GenesCCDC171
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555019
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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