A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661224



Internal ID9927329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:124465467..124469098hg38UCSC Ensembl
Outerchr7:124465310..124469251hg38UCSC Ensembl
Innerchr7:124105521..124109152hg19UCSC Ensembl
Outerchr7:124105364..124109305hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg383942
hg193942
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5403353
SamplesHG01133
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661224
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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