A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656481



Internal ID2889568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:6254204..6256825hg38UCSC Ensembl
Outerchr6:6254047..6256978hg38UCSC Ensembl
Innerchr6:6254437..6257058hg19UCSC Ensembl
Outerchr6:6254280..6257211hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg382932
hg192932
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6564001
SamplesNA19437
Known GenesF13A1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656481
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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