A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5989837



Internal ID21899180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:75534596..75535045hg38UCSC Ensembl
chr2:75761722..75762171hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526843
Samples
Known GenesEVA1A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5989837
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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