A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4389899



Internal ID21381034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74237007..74237168hg38UCSC Ensembl
chr11:73948052..73948213hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705156
Samples
Known GenesPPME1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4389899
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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