A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17594614



Internal ID21786657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124922266..124922331hg38UCSC Ensembl
chr10:126610835..126610900hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6014137
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17594614
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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