A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899154



Internal ID22674280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:54814725..54825498hg38UCSC Ensembl
chr5:54110553..54121326hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3810774
hg1910774
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416003
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899154
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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