A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1567608



Internal ID12384045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1592323..1592323hg38UCSC Ensembl
chr10:1634518..1634518hg19UCSC Ensembl
chr10:1624518..1624518hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3863
hg1963
hg1863
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4092313
SamplesHuRef
Known GenesADARB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1567608
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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