A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918989



Internal ID22694211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33985996..33986093hg38UCSC Ensembl
chr11:34007543..34007640hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363753
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918989
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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