A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674620



Internal ID9940725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:168370685..168374434hg38UCSC Ensembl
Outerchr1:168370648..168374484hg38UCSC Ensembl
Innerchr1:168339923..168343672hg19UCSC Ensembl
Outerchr1:168339886..168343722hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg383837
hg193837
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6456560
SamplesNA07357
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674620
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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