A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984773



Internal ID21894116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8243198..8243317hg38UCSC Ensembl
chr1:8303258..8303377hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519615
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984773
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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