A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4390857



Internal ID21381992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11993069..11993330hg38UCSC Ensembl
chr1:12053126..12053387hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15703848
Samples
Known GenesMFN2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4390857
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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