A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3390720



Internal ID15237687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5639728..5639728hg38UCSC Ensembl
Innerchr10:5639727..5639729hg38UCSC Ensembl
Outerchr10:5639678..5639778hg38UCSC Ensembl
chr10:5681691..5681691hg19UCSC Ensembl
Innerchr10:5681690..5681692hg19UCSC Ensembl
Outerchr10:5681641..5681741hg19UCSC Ensembl
chr10:5721697..5721697hg18UCSC Ensembl
Innerchr10:5721698..5721696hg18UCSC Ensembl
Outerchr10:5721647..5721747hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3865
hg1965
hg1865
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8701261
SamplesNA12878
Known GenesASB13
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3390720
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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