A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4388737



Internal ID21379872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:6730309..6730629hg38UCSC Ensembl
chr8:6587830..6588150hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15704333
Samples
Known GenesAGPAT5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4388737
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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