A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742483



Internal ID20518466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6488249..6488301hg38UCSC Ensembl
chr9:6488249..6488301hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260036
Samples
Known GenesUHRF2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742483
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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