A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030275



Internal ID21939618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28891378..28892829hg38UCSC Ensembl
chr16:28902699..28904150hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381452
hg191452
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621466
Samples
Known GenesATP2A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030275
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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