A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744171



Internal ID20520168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113900677..113900910hg38UCSC Ensembl
chr9:116662957..116663190hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277202
Samples
Known GenesZNF618
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744171
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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