A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112505



Internal ID21295771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:51266332..51721911hg38UCSC Ensembl
Innerchr8:52178892..52634471hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg38455580
hg19455580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087156
Samplessample130
Known GenesPXDNL
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112505
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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