A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661397



Internal ID9927502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:188741460..188746690hg38UCSC Ensembl
Outerchr1:188741423..188746740hg38UCSC Ensembl
Innerchr1:188710591..188715821hg19UCSC Ensembl
Outerchr1:188710554..188715871hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg385318
hg195318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5824178
SamplesHG01108
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661397
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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