A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910836



Internal ID22686048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70279753..70279904hg38UCSC Ensembl
chr11:70125859..70126010hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367327
Samples
Known GenesPPFIA1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910836
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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