A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1001078



Internal ID7066207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:89304240..89308506hg38UCSC Ensembl
Outerchr9:91919155..91923421hg19UCSC Ensembl
Outerchr9:91108975..91113241hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg383650
hg193650
hg183650
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564935
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1001078
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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