A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3363946



Internal ID15210924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133121258..133122156hg38UCSC Ensembl
Innerchr10:133121257..133122157hg38UCSC Ensembl
Outerchr10:133120258..133123156hg38UCSC Ensembl
chr10:134934762..134935660hg19UCSC Ensembl
Innerchr10:134934761..134935661hg19UCSC Ensembl
Outerchr10:134933762..134936660hg19UCSC Ensembl
chr10:134784752..134785650hg18UCSC Ensembl
Innerchr10:134785651..134784751hg18UCSC Ensembl
Outerchr10:134783752..134786650hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38899
hg19899
hg18899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv528e59
Supporting Variantsessv8687951
SamplesNA19239
Known GenesGPR123
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3363946
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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