A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925858



Internal ID22701085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:81554523..81653074hg38UCSC Ensembl
chr11:81265565..81364116hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3898552
hg1998552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358587
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925858
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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