A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033236



Internal ID21942579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31369264..31369317hg38UCSC Ensembl
chr16:31380585..31380638hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619138
Samples
Known GenesITGAX
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033236
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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