A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1009027



Internal ID6721131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:149380127..149381287hg38UCSC Ensembl
Outerchr3:149097914..149099074hg19UCSC Ensembl
Outerchr3:150580604..150581764hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg382502
hg192502
hg182502
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564403
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1009027
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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