A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6366678



Internal ID9350527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:18319481..18321895hg38UCSC Ensembl
Outerchr6:18319444..18321945hg38UCSC Ensembl
Innerchr6:18319712..18322126hg19UCSC Ensembl
Outerchr6:18319675..18322176hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382502
hg192502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663345
Supporting Variants
SamplesNA18546
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6366678
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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