A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3307007



Internal ID14807269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112515376..112515377hg38UCSC Ensembl
Innerchr10:112515354..112515399hg38UCSC Ensembl
Outerchr10:112515353..112515400hg38UCSC Ensembl
chr10:114275135..114275136hg19UCSC Ensembl
Innerchr10:114275113..114275158hg19UCSC Ensembl
Outerchr10:114275112..114275159hg19UCSC Ensembl
chr10:114265125..114265126hg18UCSC Ensembl
Innerchr10:114265148..114265103hg18UCSC Ensembl
Outerchr10:114265102..114265149hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38279
hg19279
hg18279
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7763865
SamplesNA19143
Known GenesVTI1A
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3307007
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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