A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661194



Internal ID9580613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28275775..28283753hg38UCSC Ensembl
Outerchr10:28275618..28283906hg38UCSC Ensembl
Innerchr10:28564704..28572682hg19UCSC Ensembl
Outerchr10:28564547..28572835hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg388289
hg198289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5396510, essv6401067, essv5595042, essv5902449, essv6172249, essv5779340, essv5764771, essv5807224
SamplesNA19437, NA19093, NA18489, NA19908, NA19457, NA19332, NA19446, HG00641
Known GenesMPP7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661194
Frequency
Sample Size1151
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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