A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17120012



Internal ID21474573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1866699..1866803hg38UCSC Ensembl
chr5:1866813..1866917hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5571798
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17120012
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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