A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740122



Internal ID20516097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:39101380..39113063hg38UCSC Ensembl
chr2:39328521..39340204hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3811684
hg1911684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295460
Samples
Known GenesSOS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740122
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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