A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116152



Internal ID21299418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39476702..39501228hg38UCSC Ensembl
Innerchr8:39334221..39358747hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3824527
hg1924527
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14086225
Samplessample254
Known GenesADAM3A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116152
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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