A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984961



Internal ID21894304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84628120..84628258hg38UCSC Ensembl
chr1:85093803..85093941hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535640
Samples
Known GenesC1orf180
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984961
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer