A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15746352



Internal ID21385901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47545907..47547065hg38UCSC Ensembl
chr11:47567459..47568617hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381159
hg191159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4431535
Supporting Variants
SamplesMDQ010
Known GenesCELF1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15746352
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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