A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16929416



Internal ID20335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:10002306..10002348hg38UCSC Ensembl
chr3:10043990..10044032hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5537441
Supporting Variants
Samples
Known GenesEMC3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16929416
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.19232


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