A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676886



Internal ID9942991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:110030202..110031031hg38UCSC Ensembl
Outerchr10:110030045..110031184hg38UCSC Ensembl
Innerchr10:111789960..111790789hg19UCSC Ensembl
Outerchr10:111789803..111790942hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg381140
hg191140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5697566, essv6242287, essv6225485, essv6351953, essv5637589, essv6030239, essv6594676, essv6459001, essv6319919, essv6582485, essv5511140, essv6537037, essv5874377, essv6093581, essv6084989, essv5489835, essv6400376, essv6065503, essv6501254, essv6212514, essv5943432, essv6005909, essv6506037, essv5903581
SamplesHG00187, NA20802, HG00367, HG00177, NA20806, NA20769, HG00281, NA20759, NA20775, HG00232, HG00282, NA20809, NA20521, NA20536, NA12718, HG00273, HG00285, HG01113, HG01137, HG00319, HG00256, NA18615, HG00125, HG00377
Known GenesADD3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676886
Frequency
Sample Size1151
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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