A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661096



Internal ID9927201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15608596..15611731hg38UCSC Ensembl
chr1:15935091..15938226hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg383136
hg193136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6487434, essv5802283, essv6566730, essv6248093
SamplesNA18510, NA19235, NA19172, NA18499
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661096
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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