A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17596136



Internal ID21788179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131108422..131108482hg38UCSC Ensembl
chr10:132906685..132906745hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6005525
Supporting Variants
Samples
Known GenesTCERG1L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17596136
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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