A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677181



Internal ID9943286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:153823657..153828642hg38UCSC Ensembl
Outerchr7:153823620..153828692hg38UCSC Ensembl
Innerchr7:153520742..153525727hg19UCSC Ensembl
Outerchr7:153520705..153525777hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg385073
hg195073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6001210
SamplesNA19449
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677181
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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