A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656628



Internal ID9922733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:273803..295043hg38UCSC Ensembl
chr7:313769..335009hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3821241
hg1921241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5786826, essv5854119
SamplesNA18543, NA18549
Known GenesLOC100288524
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656628
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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