A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676964



Internal ID9943069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:127367274..127369382hg38UCSC Ensembl
Outerchr10:127367228..127369445hg38UCSC Ensembl
Innerchr10:129165538..129167646hg19UCSC Ensembl
Outerchr10:129165492..129167709hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg382218
hg192218
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6367056
SamplesNA18561
Known GenesDOCK1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676964
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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