A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009992



Internal ID21919335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129779908..129780076hg38UCSC Ensembl
chr10:131578172..131578340hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593838
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009992
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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