A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665228



Internal ID9931333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:9645830..9727886hg38UCSC Ensembl
Outerchr7:9645793..9727936hg38UCSC Ensembl
Innerchr7:9685460..9767515hg19UCSC Ensembl
Outerchr7:9685423..9767565hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3882144
hg1982143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5864964
SamplesHG00475
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665228
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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