A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3949592



Internal ID21369661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70407972..70407972hg38UCSC Ensembl
chr10:72167728..72167728hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38375
hg19375
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15190430
SamplesHG002
Known GenesEIF4EBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3949592
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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