A curated catalogue of human genomic structural variation




Variant Details

Variant: esv991631



Internal ID7077420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:109812361..109818466hg38UCSC Ensembl
chr10:111572119..111578224hg19UCSC Ensembl
chr10:111562109..111568214hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg386106
hg196106
hg186106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv16e180
Supporting Variantsessv3585567
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv991631
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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