A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984053



Internal ID21893396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36159341..36166022hg38UCSC Ensembl
chr1:36624942..36631623hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg386682
hg196682
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17521148
Samples
Known GenesMAP7D1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984053
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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