A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622739



Internal ID6662908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28153218..28157119hg38UCSC Ensembl
Innerchr10:28153368..28156969hg38UCSC Ensembl
Outerchr10:28153068..28157269hg38UCSC Ensembl
chr10:28442147..28446048hg19UCSC Ensembl
Innerchr10:28442297..28445898hg19UCSC Ensembl
Outerchr10:28441997..28446198hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg383902
hg193902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13737819
SamplesHG01948
Known GenesMPP7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622739
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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