A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4389399



Internal ID21380534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59691182..59692355hg38UCSC Ensembl
chr10:61450940..61452113hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg381174
hg191174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15704879
Samples
Known GenesSLC16A9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4389399
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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