A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956825



Internal ID22731981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:85818864..85818864hg38UCSC Ensembl
chr3:85868014..85868014hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417093
Samples
Known GenesCADM2, CADM2-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956825
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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