A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661301



Internal ID9927406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:178978976..179006477hg38UCSC Ensembl
Outerchr1:178978939..179006527hg38UCSC Ensembl
Innerchr1:178948111..178975612hg19UCSC Ensembl
Outerchr1:178948074..178975662hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3827589
hg1927589
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6519400
SamplesNA19079
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661301
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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