A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674698



Internal ID9940803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:100553178..100556500hg38UCSC Ensembl
Outerchr13:100553144..100556535hg38UCSC Ensembl
Innerchr13:101205432..101208754hg19UCSC Ensembl
Outerchr13:101205398..101208789hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg383392
hg193392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv377e199
Supporting Variantsessv5871802, essv5886794
SamplesNA19059, HG00580
Known GenesGGACT
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674698
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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