A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5983825



Internal ID21893168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31481248..31485812hg38UCSC Ensembl
chr1:31954095..31958659hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg384565
hg194565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17518676
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5983825
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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