A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748846



Internal ID20524873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:1443731..1443798hg38UCSC Ensembl
chr2:1447503..1447570hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262463
Samples
Known GenesTPO
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748846
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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