A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5838472



Internal ID8815875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:67468143..68425607hg38UCSC Ensembl
chr7:66933130..67890594hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38957465
hg19957465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2678425
Supporting Variants
SamplesNA20756
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5838472
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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