A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668886



Internal ID9588305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:71603858..71604035hg38UCSC Ensembl
chr7:71068843..71069020hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6043930, essv6237529, essv6343741, essv6384907, essv5602350, essv5929954, essv6101149, essv5536528, essv5795938, essv6129646, essv5673656, essv6260931, essv6471495, essv6598103, essv6281287, essv5831117, essv5943527, essv5553337, essv6071970, essv6047709, essv6197079, essv6408832, essv5765068, essv6171731, essv5580754, essv5615745, essv6021446, essv5856638, essv5947501, essv6310544, essv5985801, essv6056381, essv6137399, essv6224837, essv5989698, essv5971349, essv5705868, essv6461847, essv6588845, essv5750480, essv6331421, essv5856464, essv6498658, essv6164361, essv5490415
SamplesHG00344, HG01072, HG01173, HG00310, HG00261, HG00707, HG01389, HG01492, HG01082, HG00428, HG00375, HG01350, HG00139, HG00701, HG00335, HG00253, HG00154, HG00250, HG01375, HG01048, HG00315, HG00125, NA19377, HG00108, NA19703, HG01066, NA06986, HG01073, HG00232, HG00277, NA18613, HG00329, NA19707, HG00246, HG01060, NA18910, HG01383, HG00427, HG00443, HG00123, HG00137, HG00271, HG00136, HG00126, HG01354
Known GenesWBSCR17
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668886
Frequency
Sample Size1151
Observed Gain0
Observed Loss45
Observed Complex0
Frequencyn/a


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