A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885329



Internal ID22660313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45986685..45986764hg38UCSC Ensembl
chr1:46452357..46452436hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389001
Samples
Known GenesMAST2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885329
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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