A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3408497



Internal ID14908773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:47008246..47149644hg19UCSC Ensembl
Innerchr10:47009246..47148644hg19UCSC Ensembl
Outerchr10:47007246..47150644hg19UCSC Ensembl
chr10:46428252..46569650hg18UCSC Ensembl
Innerchr10:46429252..46568650hg18UCSC Ensembl
Outerchr10:46427252..46570650hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19141399
hg18141399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv409e59
Supporting Variantsessv8688074
SamplesNA19238
Known GenesHNRNPA1P33, LINC00842, LOC100996758, NPY4R
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3408497
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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