A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4390153



Internal ID21381288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:14792453..14792574hg38UCSC Ensembl
chr12:14945387..14945508hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705296
Samples
Known GenesWBP11
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4390153
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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