A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5648898



Internal ID21597203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:2727789..2727789hg38UCSC Ensembl
chr20:2708435..2708435hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg383706
hg193706
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116206
SamplesHG00731
Known GenesEBF4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5648898
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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