A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736500



Internal ID20512449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:28335881..28338220hg38UCSC Ensembl
chr2:28558748..28561087hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg382340
hg192340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275032
Samples
Known GenesBRE
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736500
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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