A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117011



Internal ID21300277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:156909717..156919879hg38UCSC Ensembl
Innerchr6:157230851..157241013hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3810163
hg1910163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1079n145
Supporting Variantsnssv14083033
Samplessample343
Known GenesARID1B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117011
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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