A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7768486



Internal ID13616877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110418010..110418011hg38UCSC Ensembl
Innerchr10:110417988..110418033hg38UCSC Ensembl
Outerchr10:110417987..110418034hg38UCSC Ensembl
chr10:112177768..112177769hg19UCSC Ensembl
Innerchr10:112177746..112177791hg19UCSC Ensembl
Outerchr10:112177745..112177792hg19UCSC Ensembl
chr10:112167758..112167759hg18UCSC Ensembl
Innerchr10:112167781..112167736hg18UCSC Ensembl
Outerchr10:112167735..112167782hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg385580
hg195580
hg185580
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3304971
Supporting Variants
SamplesNA12872
Known Genes
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7768486
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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