A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5701656



Internal ID9031771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:22029251..22029274hg38UCSC Ensembl
Outerchr7:22029094..22029427hg38UCSC Ensembl
Innerchr7:22068869..22068892hg19UCSC Ensembl
Outerchr7:22068712..22069045hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2669489
Supporting Variants
SamplesHG00657
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5701656
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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