A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17350169



Internal ID22575838
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 StatusS
Merged Variantsnsv5909090
Supporting Variants
Samples
Known GenesFAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17350169
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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