A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658488



Internal ID9924593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:36671764..36672643hg38UCSC Ensembl
Outerchr13:36671607..36672796hg38UCSC Ensembl
Innerchr13:37245901..37246780hg19UCSC Ensembl
Outerchr13:37245744..37246933hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381190
hg191190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6007153
SamplesHG00543
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658488
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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