A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984094



Internal ID21893437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40277373..40285273hg38UCSC Ensembl
chr1:40743045..40750945hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg387901
hg197901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17529897
Samples
Known GenesZMPSTE24
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984094
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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