A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4391405



Internal ID21382435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:115007564..115010717hg38UCSC Ensembl
chr4:115928720..115931873hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg383154
hg193154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15703198
Samples
Known GenesNDST4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4391405
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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