A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676407



Internal ID9942512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65582308..65585614hg38UCSC Ensembl
Outerchr10:65581937..65585984hg38UCSC Ensembl
Innerchr10:67342066..67345372hg19UCSC Ensembl
Outerchr10:67341695..67345742hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg384048
hg194048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5512417, essv6086690, essv6433473, essv6294454, essv6128210, essv6069337, essv6138974, essv5609783, essv5593323, essv5948605, essv5529306, essv5827627, essv6137935, essv6027776
SamplesNA19332, NA19396, NA19319, NA19457, NA19455, NA19449, NA19318, NA19436, NA19434, NA19334, NA19467, NA19472, NA19429, NA19346
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676407
Frequency
Sample Size1151
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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