A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5983037



Internal ID21892380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23926957..23931242hg38UCSC Ensembl
chr1:24253447..24257732hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg384286
hg194286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17530736
Samples
Known GenesMIR378F
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5983037
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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