A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050298



Internal ID21959531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10586278..10593490hg38UCSC Ensembl
chr21:10918967..10926179hg19UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg387213
hg197213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17643018
Samples
Known GenesTPTE
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050298
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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