A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4392267



Internal ID21383297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:19814598..19820989hg38UCSC Ensembl
chr6:19814829..19821220hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg386392
hg196392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15703721
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4392267
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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