A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662882



Internal ID9582301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4622100..4622412hg38UCSC Ensembl
chr16:4672101..4672413hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5487774, essv6509403, essv6394546, essv6556709, essv6270876, essv6286855, essv5824095, essv5763673, essv6116157, essv6485974, essv6277284, essv6525890, essv6219624, essv5620255, essv5492824, essv6082149, essv5822885, essv5653206, essv5969123, essv5693519, essv6095024, essv6257174, essv6477904, essv6587682, essv6433577, essv6196035, essv6084518, essv6332201, essv6182822, essv5817815, essv5688315, essv6169482, essv5478628, essv6362448, essv5985958, essv6555698, essv5589202, essv5794969, essv6436254, essv6199468, essv6163869
SamplesNA18502, NA19704, NA19819, NA19377, NA18870, NA19920, NA20806, NA19374, NA19373, NA19076, NA18519, NA19313, HG01365, NA19384, NA19130, NA19404, NA18874, NA19372, NA19901, NA20757, NA19347, NA19391, NA19455, NA18516, NA19257, NA19395, NA19401, HG00476, NA19321, NA19331, HG01375, NA19428, NA19818, NA19376, NA19398, NA19438, NA19093, NA19102, NA19213, HG01125, NA18511
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662882
Frequency
Sample Size1151
Observed Gain0
Observed Loss41
Observed Complex0
Frequencyn/a


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