A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922066



Internal ID22697291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32587142..32588590hg38UCSC Ensembl
chr11:32608688..32610136hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381449
hg191449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354910
Samples
Known GenesEIF3M
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922066
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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