A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657747



Internal ID9923852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:108234286..108237469hg38UCSC Ensembl
Outerchr6:108234249..108237519hg38UCSC Ensembl
Innerchr6:108555490..108558673hg19UCSC Ensembl
Outerchr6:108555453..108558723hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg383271
hg193271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5421872
SamplesNA19982
Known GenesSNX3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657747
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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