A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17525131



Internal ID21849489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:179234518..179236226hg38UCSC Ensembl
chr2:180099245..180100953hg19UCSC Ensembl
Cytoband2q31.2
Allele length
AssemblyAllele length
hg381709
hg191709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5986856
Supporting Variants
Samples
Known GenesSESTD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17525131
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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