A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5990514



Internal ID21899857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9291733..9291840hg38UCSC Ensembl
chr2:9431862..9431969hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522923
Samples
Known GenesASAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5990514
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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