A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9649535



Internal ID13071527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110417997..110418016hg38UCSC Ensembl
Innerchr10:110417993..110418020hg38UCSC Ensembl
Outerchr10:110417974..110418039hg38UCSC Ensembl
chr10:112177755..112177774hg19UCSC Ensembl
Innerchr10:112177751..112177778hg19UCSC Ensembl
Outerchr10:112177732..112177797hg19UCSC Ensembl
chr10:112167745..112167764hg18UCSC Ensembl
Innerchr10:112167768..112167741hg18UCSC Ensembl
Outerchr10:112167722..112167787hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg386000
hg196000
hg186000
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3333812
Supporting Variants
SamplesNA07347
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9649535
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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