A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982102



Internal ID21891445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:183477562..183477692hg38UCSC Ensembl
chr1:183446697..183446827hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17533682
Samples
Known GenesSMG7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982102
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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