A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5985472



Internal ID21894815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9832159..9833322hg38UCSC Ensembl
chr1:9892217..9893380hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381164
hg191164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17533659
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5985472
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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