A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5960240



Internal ID22735241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157304038..157304038hg38UCSC Ensembl
chr3:157021827..157021827hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418023
Samples
Known GenesVEPH1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5960240
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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