A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582972



Internal ID21531490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21053280..21053492hg38UCSC Ensembl
chr1:21379773..21379985hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17062242
SamplesHG03065
Known GenesEIF4G3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582972
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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