A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17552612



Internal ID21876967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:181542641..181555393hg38UCSC Ensembl
chr3:181260429..181273181hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3812753
hg1912753
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5992395
Supporting Variants
Samples
Known GenesSOX2-OT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17552612
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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