A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17550741



Internal ID21875096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155125284..155125341hg38UCSC Ensembl
chr3:154843073..154843130hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5991631
Supporting Variants
Samples
Known GenesMME
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17550741
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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