A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5983284



Internal ID21892627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24852252..24857536hg38UCSC Ensembl
chr1:25178743..25184027hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg385285
hg195285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17536441
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5983284
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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