A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980702



Internal ID21890045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:103236896..103270858hg38UCSC Ensembl
chr1:103702452..103736414hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3833963
hg1933963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17533168
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5980702
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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