A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4388868



Internal ID21380003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94792500..94792904hg38UCSC Ensembl
chr8:95804728..95805132hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15704478
Samples
Known GenesDPY19L4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4388868
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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