A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6477613



Internal ID9455016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:113470113..113470877hg38UCSC Ensembl
Outerchr7:113470076..113470927hg38UCSC Ensembl
Innerchr7:113110168..113110932hg19UCSC Ensembl
Outerchr7:113110131..113110982hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38852
hg19852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2663108
Supporting Variants
SamplesNA19834
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6477613
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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