A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735439



Internal ID20511381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92872181..92872439hg38UCSC Ensembl
chr9:95634463..95634721hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289326
Samples
Known GenesZNF484
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735439
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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