A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431563



Internal ID21393565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64364756..64366038hg38UCSC Ensembl
chr11:64132228..64133510hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg381283
hg191283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15752958
SamplesSMI018
Known GenesRPS6KA4
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431563
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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