A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668176



Internal ID9934281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:35692796..35696669hg38UCSC Ensembl
Outerchr13:35692639..35696822hg38UCSC Ensembl
Innerchr13:36266933..36270806hg19UCSC Ensembl
Outerchr13:36266776..36270959hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg384184
hg194184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5899914
SamplesNA12717
Known GenesMIR548F5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668176
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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