A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5986929



Internal ID21896272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:17853116..17853264hg38UCSC Ensembl
chr2:18034383..18034531hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522771
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5986929
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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