A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663696



Internal ID9929801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15915711..15921763hg38UCSC Ensembl
chr10:15957710..15963762hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg386053
hg196053
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5707933, essv5688539, essv6209900, essv5442045, essv5888623, essv6041821, essv5782061, essv5414723, essv6442864, essv5736264, essv6448801, essv6532042, essv5619716, essv6355808, essv6238947, essv5450256, essv6338234, essv6101336, essv5693013, essv5562319, essv5754301, essv5687810, essv5647379, essv5768109, essv6464752, essv6433824, essv6195176, essv5894430, essv6263989, essv6198116, essv5992990, essv6284910, essv6139603, essv5780903, essv5576637, essv5567058, essv6309495, essv6140677, essv5946240, essv5977029, essv5913463, essv6252085, essv5555459, essv6395566, essv6033479, essv6024160, essv6581250, essv5571041, essv6088014, essv5619574, essv6348040, essv5518930, essv5434865
SamplesNA19394, HG00542, HG00536, HG00608, NA19466, NA18508, NA19399, NA19819, NA19393, HG00566, NA18870, NA18510, NA19373, NA18940, HG01366, HG01070, HG01067, NA19383, NA19371, NA19235, NA19471, NA18986, NA19002, NA19456, NA19445, NA18867, NA19921, HG00560, NA19908, HG00557, NA19391, NA19236, HG00436, HG00533, HG01047, HG00651, NA19453, NA18853, NA19469, NA18909, NA19712, NA19444, HG01174, NA19470, NA19360, NA19085, HG00620, NA20341, NA19818, HG00421, NA19102, NA19900, HG01082
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663696
Frequency
Sample Size1151
Observed Gain0
Observed Loss53
Observed Complex0
Frequencyn/a


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