A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083589



Internal ID21286463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:156910075..156919122hg38UCSC Ensembl
Innerchr6:157231209..157240256hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg389048
hg199048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111712
Supporting Variants
Samplessample39
Known GenesARID1B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083589
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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