A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3432601



Internal ID14932871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1616357..1617855hg38UCSC Ensembl
Innerchr10:1616855..1617357hg38UCSC Ensembl
Outerchr10:1615357..1618855hg38UCSC Ensembl
chr10:1658552..1660050hg19UCSC Ensembl
Innerchr10:1659050..1659552hg19UCSC Ensembl
Outerchr10:1657552..1661050hg19UCSC Ensembl
chr10:1648552..1650050hg18UCSC Ensembl
Innerchr10:1649552..1649050hg18UCSC Ensembl
Outerchr10:1647552..1651050hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg381499
hg191499
hg181499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv345e59
Supporting Variantsessv8687994
SamplesNA19239
Known GenesADARB2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3432601
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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