A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907555



Internal ID22682765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96853886..96919979hg38UCSC Ensembl
chr11:96724886..96790979hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3866094
hg1966094
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365144
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907555
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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