A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17123203



Internal ID21479006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:108562514..108562570hg38UCSC Ensembl
chr5:107898215..107898271hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5567415
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17123203
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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