A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1006576



Internal ID7071669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101815319..101816261hg38UCSC Ensembl
chr10:103575076..103576018hg19UCSC Ensembl
chr10:103565066..103566008hg18UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38943
hg19943
hg18943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3572776
SamplesHuRef
Known GenesMGEA5
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1006576
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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