A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622741



Internal ID6662910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28214312..28222818hg38UCSC Ensembl
Innerchr10:28214336..28222794hg38UCSC Ensembl
Outerchr10:28214288..28222842hg38UCSC Ensembl
chr10:28503241..28511747hg19UCSC Ensembl
Innerchr10:28503265..28511723hg19UCSC Ensembl
Outerchr10:28503217..28511771hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg388507
hg198507
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13737822, essv13737824, essv13737821, essv13737823
SamplesHG02675, HG02759, NA19239, HG02465
Known GenesMPP7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622741
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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