A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907859



Internal ID22683069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:115664462..115665016hg38UCSC Ensembl
chr11:115535180..115535734hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38555
hg19555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357506
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907859
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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