A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735668



Internal ID20511612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14130072..14130424hg38UCSC Ensembl
chr11:14151618..14151970hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280050
Samples
Known GenesSPON1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735668
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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