A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610657



Internal ID21558962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:40192313..40192313hg38UCSC Ensembl
chr3:40233804..40233804hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17130588
SamplesHG00732
Known GenesEIF1B-AS1, MYRIP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610657
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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