A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1011312



Internal ID7060074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:98055494..98062593hg38UCSC Ensembl
Outerchr10:99815251..99822350hg19UCSC Ensembl
Outerchr10:99805241..99812340hg18UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg387100
hg197100
hg187100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565028
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1011312
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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