A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904540



Internal ID22679717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:109162813..109162942hg38UCSC Ensembl
chr5:108498514..108498643hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421634
Samples
Known GenesFER
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904540
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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