A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5571183



Internal ID21519558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176394484..176394624hg38UCSC Ensembl
chr5:175821485..175821625hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17135863
SamplesHG02011
Known GenesCLTB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5571183
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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