A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5727157



Internal ID9901231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27699134..27699693hg38UCSC Ensembl
chr13:28273271..28273830hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657159
Supporting Variants
SamplesNA20795
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5727157
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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