A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926494



Internal ID22701721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87731456..87731515hg38UCSC Ensembl
chr11:87442348..87442407hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361094
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926494
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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