A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4389307



Internal ID21380442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168584772..168584919hg38UCSC Ensembl
chr1:168554010..168554157hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15704127
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4389307
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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