A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664009



Internal ID9930114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40529727..40531388hg38UCSC Ensembl
chr15:40821926..40823587hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381662
hg191662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6268030, essv5649640, essv6541857, essv6169162, essv6347538, essv6442522, essv6391434, essv6415825, essv5409988, essv6117380, essv6487504, essv6096961, essv6168666, essv5511606, essv5670569, essv5414055, essv5501416, essv5578767, essv6138774, essv6543488, essv5656019, essv6309162, essv6428192, essv6596090, essv6398995, essv5804200, essv5593109, essv5731113
SamplesHG00306, HG00244, NA12751, NA12004, HG00737, HG01051, HG01168, HG01067, NA20811, HG00338, HG01048, HG00253, HG01136, NA19657, HG01171, NA20760, NA19776, HG00273, HG00250, NA06989, NA19756, NA18576, HG00336, HG00278, NA19783, NA20510, HG00310, HG00345
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664009
Frequency
Sample Size1151
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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