A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17350186



Internal ID22575855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:114878171..114899776hg38UCSC Ensembl
chr11:114748892..114770496hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3821606
hg1921605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5908601
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17350186
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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