A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3368232



Internal ID14868491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46242510..46249708hg38UCSC Ensembl
Innerchr10:46243510..46248708hg38UCSC Ensembl
Outerchr10:46241510..46250708hg38UCSC Ensembl
chr10:47613746..47620944hg19UCSC Ensembl
Innerchr10:47614746..47619944hg19UCSC Ensembl
Outerchr10:47612746..47621944hg19UCSC Ensembl
chr10:47083752..47090950hg18UCSC Ensembl
Innerchr10:47084752..47089950hg18UCSC Ensembl
Outerchr10:47082752..47091950hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg387199
hg197199
hg187199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8688100
SamplesNA19239
Known GenesANTXRLP1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3368232
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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