A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4389314



Internal ID21380449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27823847..27824162hg38UCSC Ensembl
chr10:28112776..28113091hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15704829
Samples
Known GenesARMC4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4389314
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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