A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624217



Internal ID7011073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92214419..92228059hg38UCSC Ensembl
Innerchr10:92214472..92228006hg38UCSC Ensembl
Outerchr10:92214366..92228112hg38UCSC Ensembl
chr10:93974176..93987816hg19UCSC Ensembl
Innerchr10:93974229..93987763hg19UCSC Ensembl
Outerchr10:93974123..93987869hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg3813641
hg1913641
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13896520
SamplesHG01149
Known GenesCPEB3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624217
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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