A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889564



Internal ID22664583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151537872..151581156hg38UCSC Ensembl
chr3:151255660..151298944hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3843285
hg1943285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414882
Samples
Known GenesMIR5186
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889564
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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