A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740982



Internal ID20516959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:40426236..40426298hg38UCSC Ensembl
chr3:40467727..40467789hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288595
Samples
Known GenesENTPD3, ENTPD3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740982
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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