A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676690



Internal ID9942795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122610228..122618312hg38UCSC Ensembl
Outerchr10:122610194..122618347hg38UCSC Ensembl
Innerchr10:124369744..124377828hg19UCSC Ensembl
Outerchr10:124369710..124377863hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg388154
hg198154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5797993, essv5929984
SamplesHG00404, NA19835
Known GenesDMBT1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676690
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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