A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924331



Internal ID22699558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67075336..67077458hg38UCSC Ensembl
chr11:66842807..66844929hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg382123
hg192123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358981
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924331
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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