A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1105125



Internal ID11921564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1373820..1373820hg38UCSC Ensembl
chr10:1416015..1416015hg19UCSC Ensembl
chr10:1406015..1406015hg18UCSC 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 Variantsessv3651866
SamplesHuRef
Known GenesADARB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1105125
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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