A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622334



Internal ID7009193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11111730..11114907hg38UCSC Ensembl
Innerchr10:11111788..11114850hg38UCSC Ensembl
Outerchr10:11111673..11114965hg38UCSC Ensembl
chr10:11153693..11156870hg19UCSC Ensembl
Innerchr10:11153751..11156813hg19UCSC Ensembl
Outerchr10:11153636..11156928hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg383178
hg193178
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13695966
SamplesHG02367
Known GenesCELF2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622334
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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