A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565486



Internal ID21513800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20807903..20807963hg38UCSC Ensembl
chr1:21134396..21134456hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17062606
SamplesHG00171
Known GenesEIF4G3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565486
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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