A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4390401



Internal ID21381536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93803647..93808914hg38UCSC Ensembl
chr12:94197423..94202690hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg385268
hg195268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705437
Samples
Known GenesCRADD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4390401
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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