A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1327835



Internal ID12144271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1473945..1473945hg38UCSC Ensembl
chr10:1516140..1516140hg19UCSC Ensembl
chr10:1506140..1506140hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3876
hg1976
hg1876
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3671651
SamplesHuRef
Known GenesADARB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1327835
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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