A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662418



Internal ID9928523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:36485926..36486199hg38UCSC Ensembl
chr5:36486028..36486301hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6482494, essv6126565, essv5656655, essv6032517, essv5813326, essv6266834, essv6308615, essv6112511, essv5503925, essv6219949, essv5576976, essv6081277, essv5574571, essv6461974, essv5968811, essv6337427, essv5885304, essv5969305, essv5851320, essv6375221, essv6385997, essv5759403, essv5456403, essv5879016, essv6467559, essv5418598, essv5650918, essv6089455, essv6492025, essv6324408, essv6559008, essv5454156, essv6403062, essv5424589, essv5750181, essv5403936, essv5830416, essv5604426, essv5848543, essv5629363, essv5583037, essv6439106, essv5824991, essv6539069, essv6042848, essv6568688, essv6106814, essv6348155, essv6004212, essv5710797, essv6091688, essv6572248, essv6041556, essv6411830, essv5839210, essv5778179, essv6526775, essv5861479, essv6002678, essv5474472, essv6317684, essv5915913, essv5522411, essv5939776, essv5864014, essv5910416, essv6503134, essv5670702, essv5482482, essv6127572, essv5661289, essv5530305, essv6377191, essv5751823, essv5715419, essv5839755, essv6430225, essv5555412, essv6392237, essv6080064, essv5629262, essv6583337, essv6483729, essv5837925, essv6153038
SamplesNA19648, NA12286, NA11995, HG00671, NA10851, HG01359, NA18980, HG01066, NA12751, NA18545, NA18870, NA12750, HG01140, HG00327, NA18944, NA18550, HG00589, HG01168, NA12891, NA18558, NA11992, NA18571, NA12287, HG00185, HG00243, HG00590, HG01080, NA12156, NA19137, NA11932, HG01072, NA19207, NA19172, NA19087, HG00309, NA12828, NA20515, NA11993, HG01124, HG00154, NA18605, NA19210, NA12489, HG00183, HG00596, HG00328, NA12003, NA12878, NA18956, HG00584, HG01390, HG00284, NA18573, NA20299, HG00250, NA19655, HG00373, NA12249, HG00525, NA18555, NA12144, HG00246, NA18570, NA18593, NA18974, NA18546, HG00611, HG00124, NA11881, NA19108, HG00357, HG00319, NA07037, NA06986, HG00478, HG00259, NA19093, HG00310, NA20807, NA20528, HG00274, HG00252, NA20322, HG00345, HG01061
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662418
Frequency
Sample Size1151
Observed Gain0
Observed Loss85
Observed Complex0
Frequencyn/a


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