A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671166



Internal ID9937271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:157495544..157505788hg38UCSC Ensembl
Outerchr7:157495387..157505941hg38UCSC Ensembl
Innerchr7:157288238..157298482hg19UCSC Ensembl
Outerchr7:157288081..157298635hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3810555
hg1910555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6342713, essv6382791
SamplesHG01072, HG00732
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671166
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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