A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5537441



Internal ID261451
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 StatusM
Merged Variants
Supporting Variantsnssv16929416
Samples
Known GenesEMC3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5537441
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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