A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17547780



Internal ID21872135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:152845443..152846981hg38UCSC Ensembl
chr3:152563232..152564770hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg381539
hg191539
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5992087
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17547780
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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