A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984363



Internal ID21893706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:49299525..49406294hg38UCSC Ensembl
chr1:49765197..49871966hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38106770
hg19106770
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17523608
Samples
Known GenesAGBL4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984363
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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