A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747372



Internal ID20523391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25261412..25261581hg38UCSC Ensembl
chr2:25484281..25484450hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277981
Samples
Known GenesDNMT3A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747372
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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