A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980646



Internal ID21889989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:107036362..107036439hg38UCSC Ensembl
chr1:107578984..107579061hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17534625
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5980646
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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