A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1006945



Internal ID7072038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:76996958..76999718hg38UCSC Ensembl
Outerchr9:79611874..79614634hg19UCSC Ensembl
Outerchr9:78801694..78804454hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382301
hg192301
hg182301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565070
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1006945
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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