A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731282



Internal ID20507201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:2905247..2905336hg38UCSC Ensembl
chr2:2909019..2909108hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262325
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731282
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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