A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4389573



Internal ID21380708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114328138..114328488hg38UCSC Ensembl
chr10:116087897..116088247hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38351
hg19351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2n171
Supporting Variantsnssv15704973
Samples
Known GenesAFAP1L2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4389573
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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