A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5480728



Internal ID258228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137196866..137198157hg38UCSC Ensembl
chr9:140091318..140092609hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg381292
hg191292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029642
Samples
Known GenesTPRN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5480728
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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