A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762475



Internal ID20538335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35403927..35403927hg38UCSC Ensembl
chr11:35425474..35425474hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38482
hg19482
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288821
Samples
Known GenesSLC1A2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762475
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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