A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1081n145



Internal ID22814097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159725977..159729732hg38UCSC Ensembl
chr6:160147009..160150764hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg383756
hg193756
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3114779, nsv3117162
Samplessample349, sample348
Known GenesWTAP
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1081n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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