A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898087



Internal ID22673198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38713272..38713495hg38UCSC Ensembl
chr3:38754763..38754986hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38224
hg19224
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419960
Samples
Known GenesSCN10A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898087
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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