A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269531



Internal ID20478749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124905127..124908393hg38UCSC Ensembl
chr11:124775023..124778289hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg383267
hg193267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735390
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269531
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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