A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4388844



Internal ID21379979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81275718..81276559hg38UCSC Ensembl
chr8:82187953..82188794hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38842
hg19842
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15704452
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4388844
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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