A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001270



Internal ID21910613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114214398..114214473hg38UCSC Ensembl
chr10:115974157..115974232hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596276
Samples
Known GenesTDRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001270
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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