A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2677848

Internal ID9597267
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27707038..27707273hg38UCSC Ensembl
chr10:27995967..27996202hg19UCSC Ensembl
Allele length
AssemblyAllele length
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
AnalysisNo reference, merging analysis
Pubmed ID23128226
Accession Number(s)esv2677848
Sample Size1151
Observed Gain0
Observed Loss80
Observed Complex0

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