A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984992



Internal ID21894335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:92897488..92903524hg38UCSC Ensembl
chr1:93363045..93369081hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg386037
hg196037
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17534240
Samples
Known GenesFAM69A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984992
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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