A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674753



Internal ID9940858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:35406109..35410248hg38UCSC Ensembl
Outerchr10:35406075..35410283hg38UCSC Ensembl
Innerchr10:35695037..35699176hg19UCSC Ensembl
Outerchr10:35695003..35699211hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg384209
hg194209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv129e199
Supporting Variantsessv5947366
SamplesNA19713
Known GenesCCNY
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674753
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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