A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918148



Internal ID22693369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116841749..116842061hg38UCSC Ensembl
chr11:116712465..116712777hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365321
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918148
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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