A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659973



Internal ID9926078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:26510505..26511114hg38UCSC Ensembl
Outerchr13:26510468..26511164hg38UCSC Ensembl
Innerchr13:27084642..27085251hg19UCSC Ensembl
Outerchr13:27084605..27085301hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38697
hg19697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6533956
SamplesHG01149
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659973
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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