A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666822



Internal ID9586241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156761501..156762764hg38UCSC Ensembl
chr1:156731293..156732556hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg381264
hg191264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6133100, essv5665567, essv5448565, essv5729764, essv6442703, essv5977697, essv5977844, essv5832386, essv6375351, essv5854977, essv6440184, essv6185398, essv6129710, essv6230607, essv6358439, essv6406145, essv5952835, essv5770936, essv6321956, essv6527766, essv6372071, essv5598979, essv6027840
SamplesNA20514, NA18510, NA07346, NA18519, NA20768, NA18964, NA11930, NA11831, NA10847, NA18871, NA18573, NA12829, NA11893, NA18499, NA18576, NA07051, NA12046, NA07037, NA12763, NA18501, NA12830, NA19102, NA18522
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666822
Frequency
Sample Size1151
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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