A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15705837



Internal ID21378113
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 StatusS
Merged Variantsnsv4389611
Supporting Variants
Samples
Known GenesEIF2B4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15705837
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0402299


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