A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667919



Internal ID9934024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2848631..2850972hg38UCSC Ensembl
chr7:2888265..2890606hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg382342
hg192342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6150471, essv6485857
SamplesNA11920, NA18873
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667919
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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