A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915452



Internal ID22690670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64228149..64239579hg38UCSC Ensembl
chr11:63995621..64007051hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3811431
hg1911431
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17349905
Samples
Known GenesDNAJC4, NUDT22, VEGFB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915452
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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