A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672608



Internal ID9592027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71931168..71932736hg38UCSC Ensembl
Outerchr15:71931011..71932889hg38UCSC Ensembl
Innerchr15:72223509..72225077hg19UCSC Ensembl
Outerchr15:72223352..72225230hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381879
hg191879
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5471834
SamplesHG00418
Known GenesMYO9A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672608
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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