A curated catalogue of human genomic structural variation




Variant Details

Variant: esv991635



Internal ID6727599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1373819..1373819hg38UCSC Ensembl
chr10:1416014..1416014hg19UCSC Ensembl
chr10:1406014..1406014hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3899
hg1999
hg1899
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3583911
SamplesHuRef
Known GenesADARB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv991635
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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