A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984038



Internal ID21893381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35391781..35391914hg38UCSC Ensembl
chr1:35857382..35857515hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17529838
Samples
Known GenesZMYM4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984038
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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