A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479480



Internal ID257003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15692186..15712762hg38UCSC Ensembl
chr9:15692184..15712760hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3820577
hg1920577
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17020641
Samples
Known GenesCCDC171
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479480
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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