A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565774



Internal ID7037156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:20706945..20710065hg38UCSC Ensembl
Outerchr14:21175104..21178224hg19UCSC Ensembl
Outerchr14:20244944..20248064hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg383020
hg193020
hg183020
Variant TypeCNV insertion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1007053
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565774
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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