A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981650



Internal ID21890993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157034217..157043664hg38UCSC Ensembl
chr1:157004009..157013456hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg389448
hg199448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17521974
Samples
Known GenesARHGEF11
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981650
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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