A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1079n145



Internal ID22814095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:156909717..156919879hg38UCSC Ensembl
chr6:157230851..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 Variants
Supporting Variantsnsv3117011, nsv3111712
Samplessample39, sample343
Known GenesARID1B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1079n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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