A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000540



Internal ID21909883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20940669..20942494hg38UCSC Ensembl
chr10:21229598..21231423hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg381826
hg191826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582401
Samples
Known GenesNEBL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000540
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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