A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916232



Internal ID22691451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:81272309..81306779hg38UCSC Ensembl
chr11:80983352..81017822hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3834471
hg1934471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17350089
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916232
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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