A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17538536



Internal ID21862891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48987421..48988641hg38UCSC Ensembl
chr3:49024854..49026074hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381221
hg191221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993496
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17538536
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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