A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4389466



Internal ID21380601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:229337680..229341193hg38UCSC Ensembl
chr1:229473427..229476940hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg383514
hg193514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705004
Samples
Known GenesCCSAP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4389466
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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