A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5627324



Internal ID21575629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38052417..38052417hg38UCSC Ensembl
chr8:37909935..37909935hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150204
SamplesHG03125
Known GenesEIF4EBP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5627324
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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