A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13796731



Internal ID851827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49405637..49411589hg38UCSC Ensembl
Innerchr10:49405646..49411580hg38UCSC Ensembl
Outerchr10:49405628..49411598hg38UCSC Ensembl
chr10:50613683..50619635hg19UCSC Ensembl
Innerchr10:50613692..50619626hg19UCSC Ensembl
Outerchr10:50613674..50619644hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg385953
hg195953
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623170
Supporting Variants
SamplesHG00445
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13796731
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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