A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675536



Internal ID9941641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135768013..135768615hg38UCSC Ensembl
chr7:135452761..135453363hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38603
hg19603
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5513588
SamplesNA12003
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675536
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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