A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4390481



Internal ID21381616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121792102..121792154hg38UCSC Ensembl
chr12:122230008..122230060hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705481
Samples
Known GenesRHOF
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4390481
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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