A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009954



Internal ID21919297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130184428..130186142hg38UCSC Ensembl
chr10:131982692..131984406hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg381715
hg191715
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585658
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009954
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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