A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4390333



Internal ID21381468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:68398009..68403109hg38UCSC Ensembl
chr12:68791789..68796889hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg385101
hg195101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705395
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4390333
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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