A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744671



Internal ID20520672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:8028242..8028309hg38UCSC Ensembl
chr2:8168372..8168439hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293624
Samples
Known GenesLINC00299
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744671
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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