A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658355



Internal ID9924460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97989391..97993239hg38UCSC Ensembl
chr15:98532621..98536469hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg383849
hg193849
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv469e199
Supporting Variantsessv6130310, essv6121240, essv5660425, essv6429552, essv6575808, essv5948767, essv6521394, essv5808023, essv5609423, essv6234384, essv5526376, essv6590714, essv6142380, essv6232672, essv6354854, essv5745566, essv6454495, essv5761844, essv5922232, essv6013329, essv6384506, essv6551785, essv6413849, essv6170954, essv5951743, essv5723200, essv5467663, essv5689812, essv5461059, essv5834710, essv6460161, essv5570144, essv5559026, essv6074345, essv6318489, essv6092582, essv6494571, essv5543044, essv6570030, essv5832370, essv5692462, essv5561407, essv6027656, essv6323250, essv6564553, essv5780376, essv5733478, essv5621505, essv5537302, essv6244516, essv5918374
SamplesNA18502, NA18861, NA19399, NA19914, NA19704, NA18486, NA19393, NA18504, NA18870, NA19920, NA19374, NA19373, NA19448, NA19197, NA19404, NA19720, NA20278, NA18868, NA19137, NA19172, NA19239, NA19451, NA19210, NA19437, NA19462, NA19347, NA19152, NA19982, NA18910, NA18907, HG01047, NA19114, NA18856, NA19452, NA19225, NA18523, NA19401, NA18909, NA19108, NA19434, NA19444, NA19380, NA19428, NA19324, NA19467, NA20348, NA19093, NA19213, NA19129, NA18511, NA18522
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658355
Frequency
Sample Size1151
Observed Gain0
Observed Loss51
Observed Complex0
Frequencyn/a


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