A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018419



Internal ID21927762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23229248..23234300hg38UCSC Ensembl
chr10:23518177..23523229hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg385053
hg195053
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17591395
Samples
Known GenesC10orf115
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018419
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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