A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5488998



Internal ID266290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71950970..71959343hg38UCSC Ensembl
chr9:74565886..74574259hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg388374
hg198374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv545n206
Supporting Variantsnssv17024283
Samples
Known GenesC9orf85
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5488998
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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