A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624400



Internal ID7011256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102529907..102531207hg38UCSC Ensembl
Innerchr10:102529957..102530970hg38UCSC Ensembl
Outerchr10:102529701..102531413hg38UCSC Ensembl
chr10:104289664..104290964hg19UCSC Ensembl
Innerchr10:104289714..104290727hg19UCSC Ensembl
Outerchr10:104289458..104291170hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg381301
hg191301
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13913809, essv13913805, essv13913811, essv13913810, essv13913807, essv13913803, essv13913808, essv13913806, essv13913804
SamplesNA19058, NA18964, NA18951, NA19082, NA19006, NA19077, NA18992, NA19085, NA19011
Known GenesSUFU
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624400
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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