A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579966



Internal ID21528451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:75304778..75304859hg38UCSC Ensembl
chr2:75531904..75531985hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17113648
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579966
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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