A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17349980



Internal ID22575649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123207814..123208399hg38UCSC Ensembl
chr11:123078522..123079107hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38586
hg19586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5911955
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17349980
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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