A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5957402



Internal ID22732520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:197070565..197070565hg38UCSC Ensembl
chr3:196797436..196797436hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424554
Samples
Known GenesDLG1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5957402
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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