A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672715



Internal ID9938820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:102750223..102751723hg38UCSC Ensembl
Outerchr10:102750186..102751773hg38UCSC Ensembl
Innerchr10:104509980..104511480hg19UCSC Ensembl
Outerchr10:104509943..104511530hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg381588
hg191588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5748546
SamplesHG00262
Known GenesWBP1L
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672715
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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