A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624359



Internal ID7011215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100420032..100420613hg38UCSC Ensembl
Innerchr10:100420032..100420613hg38UCSC Ensembl
Outerchr10:100419707..100420709hg38UCSC Ensembl
chr10:102179789..102180370hg19UCSC Ensembl
Innerchr10:102179789..102180370hg19UCSC Ensembl
Outerchr10:102179464..102180466hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg38582
hg19582
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13912969, essv13912968, essv13912971, essv13912966, essv13912962, essv13912967, essv13912963, essv13912973, essv13912965, essv13912970, essv13912964, essv13912972
SamplesNA19393, NA19190, HG03342, HG02645, HG02461, NA19984, NA18915, HG02666, HG01958, HG03432, HG02462, NA19030
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624359
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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