A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981795



Internal ID21891138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:182691674..182699593hg38UCSC Ensembl
chr1:182660809..182668728hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg387920
hg197920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3n212
Supporting Variantsnssv17531173
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981795
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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