A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5952687



Internal ID22680579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:51709719..51709719hg38UCSC Ensembl
chr3:51743735..51743735hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424758
Samples
Known GenesGRM2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5952687
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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