A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431498



Internal ID21393500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33037651..33038541hg38UCSC Ensembl
chr11:33059197..33060087hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38891
hg19891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15752236
SamplesMDQ025
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431498
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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