A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579759



Internal ID21528241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:29644116..29644204hg38UCSC Ensembl
chr5:29644223..29644311hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120230
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579759
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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