A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14085269



Internal ID21271225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:85234738..85248648hg38UCSC Ensembl
Innerchr8:86146967..86160877hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3813911
hg1913911
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113418
Supporting Variants
Samplessample160
Known GenesCA13
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14085269
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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