A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4390832



Internal ID21381967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:5489738..5490089hg38UCSC Ensembl
chr1:5549798..5550149hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15703293
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4390832
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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