A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5949954



Internal ID22725393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57578465..57578465hg38UCSC Ensembl
chr3:57564192..57564192hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424990
Samples
Known GenesARF4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5949954
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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