A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888882



Internal ID22663892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:127810847..127811263hg38UCSC Ensembl
chr3:127529690..127530106hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38417
hg19417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17393492
Samples
Known GenesMGLL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888882
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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