A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909090



Internal ID22684300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92444670..92456850hg38UCSC Ensembl
chr11:92177836..92190016hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3812181
hg1912181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17350169
Samples
Known GenesFAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909090
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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