A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5570471



Internal ID21518837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21053730..21053856hg38UCSC Ensembl
chr1:21380223..21380349hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17062244
SamplesHG02011
Known GenesEIF4G3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5570471
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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