A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923332



Internal ID22698559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61253366..61256023hg38UCSC Ensembl
chr11:61020838..61023495hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg382658
hg192658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356649
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923332
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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