A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110179



Internal ID21293445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:8441572..8468444hg38UCSC Ensembl
Innerchr6:8441805..8468677hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3826873
hg1926873
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087720
Samplessample222
Known GenesLOC100506207
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110179
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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