A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114779



Internal ID21298045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:159725977..159729732hg38UCSC Ensembl
Innerchr6:160147009..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 Variantsdgv1081n145
Supporting Variantsnssv14083051
Samplessample348
Known GenesWTAP
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114779
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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