A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660031



Internal ID9926136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68852313..68864038hg38UCSC Ensembl
chr10:70612069..70623794hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3811726
hg1911726
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv151e199
Supporting Variantsessv6587931
SamplesHG01066
Known GenesSTOX1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660031
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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