A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5957528



Internal ID22732643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:55952176..55952176hg38UCSC Ensembl
chr3:55986204..55986204hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416941
Samples
Known GenesERC2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5957528
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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