A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639211



Internal ID21587516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37894725..37894725hg38UCSC Ensembl
chr8:37752243..37752243hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17147840
SamplesHG03125
Known GenesRAB11FIP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639211
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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