A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17612763



Internal ID21804810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116769940..116769999hg38UCSC Ensembl
chr11:116640656..116640715hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6024789
Supporting Variants
Samples
Known GenesBUD13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17612763
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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