A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010550



Internal ID21919893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132979490..132979827hg38UCSC Ensembl
chr8:133991735..133992072hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578472
Samples
Known GenesTG
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010550
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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