A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916493



Internal ID22691712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120182897..120189091hg38UCSC Ensembl
chr11:120053605..120059799hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg386195
hg196195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362023
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916493
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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