A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431564



Internal ID21393566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65418530..65432529hg38UCSC Ensembl
chr11:65186001..65200000hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3814000
hg1914000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15752445
SamplesSMI041
Known GenesNEAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431564
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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