A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1005935



Internal ID7071029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:20638603..20642025hg38UCSC Ensembl
Outerchr9:20638602..20642024hg19UCSC Ensembl
Outerchr9:20628602..20632024hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg383450
hg193450
hg183450
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565744
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1005935
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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