A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16929414



Internal ID20334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:10002298..10002301hg38UCSC Ensembl
chr3:10043982..10043985hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5535136
Supporting Variants
Samples
Known GenesEMC3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16929414
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.012957


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