A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017851



Internal ID21927194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4815526..4815630hg38UCSC Ensembl
chr10:4857718..4857822hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17589387
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017851
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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