A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663740



Internal ID9929845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45398619..45398712hg38UCSC Ensembl
chr11:45420169..45420262hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5595496, essv6203296, essv6455523, essv6505559
SamplesNA11918, NA07347, NA19657, HG00701
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663740
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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