A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664488



Internal ID9930593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:86174649..86233998hg38UCSC Ensembl
Outerchr7:86174612..86234048hg38UCSC Ensembl
Innerchr7:85803965..85863314hg19UCSC Ensembl
Outerchr7:85803928..85863364hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3859437
hg1959437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6571285
SamplesHG00592
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664488
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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