A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673131



Internal ID9939236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142756016..142766913hg38UCSC Ensembl
chr7:142463867..142474761hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3810898
hg1910895
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6368921
SamplesHG00255
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673131
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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