A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662053



Internal ID9581472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28777366..28780020hg38UCSC Ensembl
chr7:28816983..28819637hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg382655
hg192655
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6114359
SamplesNA07051
Known GenesCREB5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662053
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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