A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677848



Internal ID9597267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27707038..27707273hg38UCSC Ensembl
chr10:27995967..27996202hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5833306, essv6261220, essv6139731, essv5629688, essv6100229, essv6570459, essv5875861, essv5783982, essv5625188, essv6144127, essv5807477, essv5755709, essv5702471, essv6064717, essv6362499, essv5601513, essv5521926, essv6380056, essv5829421, essv5814844, essv5478086, essv6376737, essv5904552, essv6277501, essv5473905, essv5976419, essv6235468, essv5854226, essv6188422, essv6013492, essv6093347, essv6050003, essv6241324, essv6546599, essv6182636, essv5514150, essv5542675, essv5536563, essv5672633, essv6183227, essv5496940, essv5791254, essv5772813, essv5799814, essv5797340, essv6283202, essv6536489, essv5493617, essv5449296, essv5831267, essv5982465, essv6197306, essv6546837, essv5864089, essv6024178, essv6116436, essv5663394, essv6274429, essv5611727, essv5859390, essv5845298, essv5406517, essv6105702, essv5629574, essv5680178, essv6385949, essv5869419, essv6003006, essv5470601, essv5674366, essv6283920, essv5749167, essv5556954, essv5963059, essv6110035, essv6365351, essv5543487, essv6442732, essv5546736, essv5453079
SamplesHG00613, NA18964, HG00313, HG00537, HG00607, NA18534, NA18530, HG00418, NA18561, NA18612, HG00731, NA18550, NA18603, HG00657, NA18953, HG01488, NA19010, NA18608, NA18541, NA18546, HG00557, NA18557, NA18943, NA18626, NA19057, NA19068, NA18576, NA18960, NA18618, HG01061, NA18991, HG00330, NA19066, NA18609, NA18547, HG00634, NA18634, NA19000, NA18572, HG00325, NA18986, HG00559, HG00560, NA18558, NA18977, HG00501, HG00672, HG01069, NA18942, HG00513, HG00524, HG00512, HG01070, HG00525, NA18985, NA18543, NA18999, HG00595, NA18552, NA18983, NA18567, NA18989, HG00580, NA18544, NA18577, NA18944, NA19063, HG00708, NA18611, HG00625, NA18549, NA19079, HG00626, HG00684, HG00671, HG00272, HG00704, NA18555, NA19065, HG00531
Known GenesMKX
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677848
Frequency
Sample Size1151
Observed Gain0
Observed Loss80
Observed Complex0
Frequencyn/a


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