A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898755



Internal ID22673876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:54473656..54494037hg38UCSC Ensembl
chr5:53769486..53789867hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3820382
hg1920382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425602
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898755
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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