A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663481



Internal ID9929586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121643732..121650030hg38UCSC Ensembl
Outerchr10:121643575..121650183hg38UCSC Ensembl
Innerchr10:123403246..123409544hg19UCSC Ensembl
Outerchr10:123403089..123409697hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg386609
hg196609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6036395, essv6325090, essv5764705, essv6101229, essv6411934, essv5998379
SamplesNA19397, NA19332, NA19776, NA19449, NA19440, NA19346
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663481
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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