A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5985196



Internal ID21894539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:85160386..85160945hg38UCSC Ensembl
chr1:85626069..85626628hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17518818
Samples
Known GenesSYDE2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5985196
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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