A curated catalogue of human genomic structural variation




Variant Details

Variant: esv998745



Internal ID6734677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1438833..1438968hg38UCSC Ensembl
chr10:1481028..1481163hg19UCSC Ensembl
chr10:1471028..1471163hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38136
hg19136
hg18136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3570713
SamplesHuRef
Known GenesADARB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv998745
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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