A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5989989



Internal ID21899332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62292645..62292789hg38UCSC Ensembl
chr2:62519780..62519924hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517998
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5989989
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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