A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13770195



Internal ID2869808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45233317..45236197hg38UCSC Ensembl
Innerchr10:45233318..45236197hg38UCSC Ensembl
Outerchr10:45233317..45236198hg38UCSC Ensembl
chr10:45728765..45731645hg19UCSC Ensembl
Innerchr10:45728766..45731645hg19UCSC Ensembl
Outerchr10:45728765..45731646hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg382881
hg192881
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623089
Supporting Variants
SamplesHG02546
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13770195
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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