A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5478216



Internal ID255779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74472359..74477063hg38UCSC Ensembl
chr9:77087275..77091979hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg384705
hg194705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025269
Samples
Known GenesMIR6130
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5478216
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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