A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918549



Internal ID22693770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129986141..129986217hg38UCSC Ensembl
chr11:129856036..129856112hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354340
Samples
Known GenesPRDM10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918549
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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