A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746269



Internal ID20522281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120609651..120622038hg38UCSC Ensembl
chr11:120480360..120492747hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3812388
hg1912388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274965
Samples
Known GenesGRIK4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746269
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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