A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658867



Internal ID9924972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:16336004..16352668hg38UCSC Ensembl
Outerchr10:16335847..16352821hg38UCSC Ensembl
Innerchr10:16378003..16394667hg19UCSC Ensembl
Outerchr10:16377846..16394820hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3816975
hg1916975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6136435, essv5676405
SamplesHG01170, HG01191
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658867
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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