A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1004136



Internal ID6716262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:5687188..5689600hg38UCSC Ensembl
Outerchr10:5729151..5731563hg19UCSC Ensembl
Outerchr10:5769157..5771569hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg383481
hg193481
hg183481
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563777
SamplesHuRef
Known GenesFAM208B
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1004136
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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