A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673478



Internal ID9592897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28214343..28222881hg38UCSC Ensembl
Innerchr10:28503272..28511810hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg388539
hg198539
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5739046, essv6044985
SamplesNA19239, NA19240
Known GenesMPP7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673478
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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