A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889837



Internal ID22664858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:100616034..100618796hg38UCSC Ensembl
chr3:100334878..100337640hg19UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg382763
hg192763
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17404941
Samples
Known GenesGPR128
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889837
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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