A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656527



Internal ID9575946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71996605..71999300hg38UCSC Ensembl
Outerchr15:71996568..71999350hg38UCSC Ensembl
Innerchr15:72288946..72291641hg19UCSC Ensembl
Outerchr15:72288909..72291691hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382783
hg192783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5676151
SamplesNA18867
Known GenesMYO9A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656527
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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