A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741875



Internal ID20517853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3734685..3734784hg38UCSC Ensembl
chr9:3734685..3734784hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16282892
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741875
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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