A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6147120



Internal ID9827661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:80485305..80485399hg38UCSC Ensembl
Outerchr6:80485028..80485675hg38UCSC Ensembl
Innerchr6:81195116..81195022hg19UCSC Ensembl
Outerchr6:81194745..81195392hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38648
hg19648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2666212
Supporting Variants
SamplesNA20314
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6147120
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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