A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4389611



Internal ID21380746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27366096..27366215hg38UCSC Ensembl
chr2:27588963..27589082hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705837
Samples
Known GenesEIF2B4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4389611
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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