A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580119



Internal ID21528606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6511439..6515401hg38UCSC Ensembl
chr5:6511552..6515514hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg383963
hg193963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17140250
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580119
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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