A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269271



Internal ID20478489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68827671..68828000hg38UCSC Ensembl
chr10:70587428..70587757hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744087
Supporting Variants
Samples
Known GenesSTOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269271
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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