A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668619



Internal ID9588038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:71452390..71461556hg38UCSC Ensembl
Outerchr13:71452356..71461591hg38UCSC Ensembl
Innerchr13:72026522..72035688hg19UCSC Ensembl
Outerchr13:72026488..72035723hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg389236
hg199236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv361e199
Supporting Variantsessv5939439
SamplesNA19712
Known GenesDACH1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668619
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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