A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292797



Internal ID20502015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110997847..110997916hg38UCSC Ensembl
chr11:110868571..110868640hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736408
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292797
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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