A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662514



Internal ID9928619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:50402295..50404058hg38UCSC Ensembl
Outerchr13:50402258..50404108hg38UCSC Ensembl
Innerchr13:50976431..50978194hg19UCSC Ensembl
Outerchr13:50976394..50978244hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg381851
hg191851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6236531
SamplesNA18596
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662514
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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