A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909829



Internal ID22685039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96895070..96906792hg38UCSC Ensembl
chr11:96766070..96777792hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3811723
hg1911723
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363654
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909829
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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