A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1004014



Internal ID7069116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:160169726..160173828hg38UCSC Ensembl
Outerchr6:160590758..160594860hg19UCSC Ensembl
Outerchr6:160510748..160514850hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg382466
hg192466
hg182466
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565505
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1004014
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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